Warbixinta Dib U Xusuusashada Daroogada

On 04/16/2025, GLENMARK PHARMACEUTICALS ayaa dib loogu yeeray CARVEDILOL 12.5 MG sababtoo ah leexashada CGMP. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Heerka II ee dib u yeerista daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: CARVEDILOL 12.5 MG
Lambarka NDC: 68462016405
Lambarka Naadiga: 17240238, 17240243, 17240245 iyo 17240248
Taariikhda uu dhacayo: Jan-26, Jan-26, Jan-26 iyo Jan-26

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacayo 1-800-FDA-0178.

On 04/16/2025, GLENMARK PHARMACEUTICALS ayaa dib loo wacay DILTIAZEM 12HR ER 120 MG leexashada CGMP awgeed. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Heerka II ee dib u yeerista daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: DILTIAZEM 12HR ER 120 MG
Lambarka NDC:68462056201
Lambarka Naadiga:17241067 iyo 17241628
Taariikhda uu dhacayo: May-26 iyo Agoosto-26

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacayo 1-800-FDA-0178.

On 04/16/2025, SOMERSET THERAPEUTICS PRIVATE LIMITED la xasuusto HALOPERIDOL DeCANOATE 100 MG/ML dammaanad la'aanta dhalmada awgeed: Warbaahintu waxay buuxisaa wasakhowga bakteeriyada. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Heerka II ee dib u yeerista daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: HALOPERIDOL DECANOATE 100 MG/ML
Lambarka NDC:70069038310
Lambarka Naadiga:A240482D
Taariikhda uu dhacayo:08/2026

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacayo 1-800-FDA-0178.

On 04/16/2025, GLENMARK PHARMACEUTICALS waxay dib u wacday LACOSAMIDE 50 MG sababtoo ah weecsanaanta CGMP. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Heerka II ee dib u yeerista daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: LACOSAMIDE 50 MG
Lambarka NDC:68462067860
Lambarka Naadiga:17240221 iyo 17240222
Taariikhda uu dhacayo:Jan-26 iyo Jan-26

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacayo 1-800-FDA-0178.

On 04/16/2025, GLENMARK PHARMACEUTICALS waxay dib u wacday LACOSAMIDE 100 MG sababtoo ah weecsanaanta CGMP. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Heerka II ee dib u yeerista daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: LACOSAMIDE 100 MG
Lambarka NDC:68462067960
Lambarka Naadiga:17232533, 17232534, 17240606, 17240619, 17240911, 17240912, 17241121 iyo 17241124
Taariikhda uu dhacayo:Nov-25, Noofambar-25, Mar-26, Mar-26, Meey-26, Meey-26, Jun-26 iyo Jun-26

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacayo 1-800-FDA-0178.

On 04/16/2025, GLENMARK PHARMACEUTICALS waxay dib u wacday LACOSAMIDE 150 MG sababtoo ah weecsanaanta CGMP. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Heerka II ee dib u yeerista daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: LACOSAMIDE 150 MG
Lambarka NDC:684620680605
Lambarka Naadiga:17241125, 17242202 iyo 17242204
Taariikhda uu dhacayo:Jun-26, Noofambar-26, Dec-26

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacayo 1-800-FDA-0178.

On 04/16/2025, GLENMARK PHARMACEUTICALS waxay dib u wacday LACOSAMIDE 200 MG sababtoo ah weecsanaanta CGMP. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Heerka II ee dib u yeerista daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: LACOSAMIDE 200 MG
Lambarka NDC:68462068160
Lambarka Naadiga:17230982, 17230986, 17231001, 17240197, 17240198, 17240215, 17240846 iyo 17240847
Taariikhda uu dhacayo:Abriil 25, Abriil 25, Abriil 25, Jan-26, Jan-26, Jan-26, Abriil 26 iyo Abriil 26

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacayo 1-800-FDA-0178.

On 04/16/2025, GLENMARK PHARMACEUTICALS waxay dib u soo celiyeen GABAPENTIN 600 MG sababtoo ah leexashada CGMP. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Heerka II ee dib u yeerista daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: GABAPENTIN 600 MG
Lambarka NDC:68462012605
Lambarka Naadiga:17231015, 17231128, 17231138, 17231139, 17231143, 17231144, 17231848, 17231898, 17231977, 17231978, 17232015 17232016, 17232017, 17232034, 17232041, 17232396, 17232406, 17232410, 17232490, 17240326, 17240327 17240383, 17240395, 17241863, 17241869, 17241870, 17231256, 17231386, 17231387, 17231407, 17231417, 17231418 17231754, 17240085 iyo 17240117
Taariikhda uu dhacayo:Apr-25, Apr-25, Abriil 25, Abriil 25, Abriil 25, Agoosto 25, Agoosto 25, Agoosto 25, Agoosto 25 – Aug-25, Agoosto-25, Agoosto-25, Agoosto 25, Agoosto 25, 25, 25, 25, 25, 25 Nov-26, 26 Nof 26, 26 Nof 26. Jan-26, Feb-26, Feb-25, Oct-25, Oct-25, Oct-25, May-25, May-25, May-25, May-25, May-25, May-25, May-XNUMX, Jul-XNUMX, Dec-XNUMX and Dec-XNUMX

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacayo 1-800-FDA-0178.

On 04/16/2025, GLENMARK PHARMACEUTICALS waxay dib u soo celiyeen NITROGLYCERIN 0.3 MG sababtoo ah leexashada CGMP. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Heerka II ee dib u yeerista daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: NITROGLYCERIN 0.3 MG
Lambarka NDC:68462063801
Lambarka Naadiga:1723236 iyo 17232367
Taariikhda uu dhacayo:Nov-25 iyo Nov-25

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacayo 1-800-FDA-0178.

On 04/16/2025, GLENMARK PHARMACEUTICALS waxay dib u soo celiyeen NITROGLYCERIN 0.4 MG sababtoo ah leexashada CGMP. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Heerka II ee dib u yeerista daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: NITROGLYCERIN 0.4 MG
Lambarka NDC:68462063945
Lambarka Naadiga:17232024, 17232071 iyo 17232072
Taariikhda uu dhacayo:Agoosto-25, Sebte-25 iyo Sebtembar-25

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacayo 1-800-FDA-0178.

On 04/16/2025, GLENMARK PHARMACEUTICALS waxay dib u soo celiyeen PRAVASTATIN SODIUM 20 MG sababtoo ah leexashada CGMP. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Heerka II ee dib u yeerista daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: PRAVASTATIN SODIUM 20 MG
Lambarka NDC:68462019605
Lambarka Naadiga:17230810, 17230811, 17230810, 17232501 iyo 17232502
Taariikhda uu dhacayo:Mar-26, Mar-26, Mar-26, Nov-26 iyo Nov-26

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacayo 1-800-FDA-0178.

On 04/16/2025, NORTHSTAR RX LLC waxay dib u wacday PRAVASTATIN SODIUM 20 MG sababo la xiriira leexinta CGMP. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Heerka II ee dib u yeerista daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: PRAVASTATIN SODIUM 20 MG
Lambarka NDC:16714055901
Lambarka Naadiga:17230810
Taariikhda uu dhacayo:Mar-26

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacayo 1-800-FDA-0178.

On 04/16/2025, NORTHSTAR RX LLC waxay dib u wacday PRAVASTATIN SODIUM 80 MG sababo la xiriira leexinta CGMP. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Heerka II ee dib u yeerista daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: PRAVASTATIN SODIUM 80 MG
Lambarka NDC:16714055901
Lambarka Naadiga:17230810
Taariikhda uu dhacayo:Mar-26

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacayo 1-800-FDA-0178.

On 04/16/2025, GLENMARK PHARMACEUTICALS waxa dib loogu yeedhay PROCHLORPERAZINE MALEATE 10 MG sababtuna waa weecan CGMP. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Heerka II ee dib u yeerista daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: PROCHLORPERAZINE MALEATE 10 MG
Lambarka NDC:68462089001
Lambarka Naadiga:17240254 iyo 17240257
Taariikhda uu dhacayo:Jan-26 iyo Jan-26

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacayo 1-800-FDA-0178.

On 04/16/2025, GLENMARK PHARMACEUTICALS waxa dib loogu yeedhay SAXAGLIPTIN HCL 2.5 MG sababtuna tahay leexashada CGMP. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Heerka II ee dib u yeerista daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: SAXAGLIPTIN HCL 2.5 MG
Lambarka NDC:68462072690
Lambarka Naadiga:17241788, 17241821 iyo 17241822
Taariikhda uu dhacayo:Sebtembar-26, Sebte-26 iyo Sebte-26

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacayo 1-800-FDA-0178.

On 04/16/2025, GLENMARK PHARMACEUTICALS waxa dib loogu yeedhay SAXAGLIPTIN HCL 5 MG sababtuna tahay leexashada CGMP. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Heerka II ee dib u yeerista daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: SAXAGLIPTIN HCL 5 MG
Lambarka NDC:68462072730
Lambarka Naadiga:17232460, 17232460, 17241194 iyo 17241194
Taariikhda uu dhacayo:Nov-25, Noofambar-25, Jun-26 iyo Jun-26

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacayo 1-800-FDA-0178.

On 04/16/2025, GLENMARK PHARMACEUTICALS waxay dib u soo celiyeen ROSUVASTATIN CALCIUM 40 MG sababtoo ah leexashada CGMP. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Heerka II ee dib u yeerista daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: ROSUVASTATIN CALCIUM 40 MG
Lambarka NDC:68462026430
Lambarka Naadiga:17240389, 17240390, 17240426, 17240427, 17240428, 17240778, 17241055, 17241074, 17241075, 17241091 iyo 17241100
Taariikhda uu dhacayo:Feb-26, Feb-26, Feb-26, Feb-26, Feb-26, Apr-26, May-26, Jun-26, Jun-26, Jun-26 iyo Jun-26

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacayo 1-800-FDA-0178.

On 04/16/2025, B. BRAUN MEDICAL INC oo dib loo soo celiyay SODIUM KHLORIDE 0.9 % iyadoo ay ugu wacan tahay Jiritaanka Maaddada Gaarka ah. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Heerka II ee dib u yeerista daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: SODIUM Kchloride 0.9 %
Lambarka NDC:00264220110
Lambarka Naadiga:J4K936
Taariikhda uu dhacayo:7/31/2027

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacayo 1-800-FDA-0178.

On 04/16/2025, GLENMARK PHARMACEUTICALS waxay dib u soo celiyeen SOLIFENACIN SUCCINATE 5 MG sababtoo ah leexashada CGMP. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Heerka II ee dib u yeerista daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: SOLIFENACIN SUCCINATE 5 MG
Lambarka NDC:68462038630
Lambarka Naadiga:17232395, 17232400 iyo 17232395
Taariikhda uu dhacayo:Nofeembar-25, Noofambar-25 iyo Noofambar-25

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacayo 1-800-FDA-0178.

On 04/16/2025, GLENMARK PHARMACEUTICALS waxay dib u soo celiyeen SOLIFENACIN SUCCINATE 5 MG sababtoo ah leexashada CGMP. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Heerka II ee dib u yeerista daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: SOLIFENACIN SUCCINATE 5 MG
Lambarka NDC:68462038690
Lambarka Naadiga:17232395, 17232400 iyo 17232395
Taariikhda uu dhacayo:Nofeembar-25, Noofambar-25 iyo Noofambar-25

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacayo 1-800-FDA-0178.

On 04/16/2025, GLENMARK PHARMACEUTICALS waxay dib u soo celiyeen SOLIFENACIN SUCCINATE 10 MG sababtoo ah leexashada CGMP. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Heerka II ee dib u yeerista daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: SOLIFENACIN SUCCINATE 10 MG
Lambarka NDC:68462038730
Lambarka Naadiga:17230762
Taariikhda uu dhacayo:Mar-25

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacayo 1-800-FDA-0178.

On 04/16/2025, PHARMACEUTICALS ZYDUS waxay dib u wacday VENLAFAXINE HCL 75 MG iyadoo ay ugu wacan tahay Jiritaanka Walxaha Ajnabiga ah: Cabashada badeecada ee la helay joogitaanka walxaha ajnabiga ah ee ku dhex jira una eg bir xiirashada hal kiniin ah. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Heerka II ee dib u yeerista daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: VENLAFAXINE HCL 75 MG
Lambarka NDC:68382002101
Lambarka Naadiga:M314265
Taariikhda uu dhacayo:10/31/2025

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacayo 1-800-FDA-0178.

On 04/02/2025, Strides Pharmacy, INC waxay dib u xasuusisay TESTOSTERONE 25MG(1%) iyadoo ay ugu wacan tahay Jiritaanka walxaha shisheeye: Joogitaanka Benzene. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Heerka II ee dib u yeerista daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: TESTOSTERONE 25MG (1%)
Lambarka NDC: 64380015102
Lambarka Naadiga: 5501127A, 5501236A, 5501341A, 5501406A, 5501408A, 5501516A, 5501568A, 5501829A, 5502000A, 5502004A, 5502005 5502092A, 5502217A iyo 5502262A
Taariikhda uu dhacayo: Apr-25, Jun-25, Jul-25, Agoosto-25, Sebte-25, Oct-25, Mar-26, Jul-26, Aug-26, Oct-26, Dec-26 iyo Jan-27

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun xun ee ka yimaada isticmaalka dawooyinka dhakhtarku qoray waa in lagu wargeliyaa FDA adigoo booqanaya www.fda.gov/medwatch/report.htm ama wac 1-800-FDA-0178.

On 04/02/2025, Strides Pharma, INC waxay dib u wacday TESTOSTERONE 50 MG (1%) iyadoo ay ugu wacan tahay Jiritaanka walxaha shisheeye: Joogitaanka Benzene. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Heerka II ee dib u yeerista daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: TESTOSTERONE 50 MG (1%)
Lambarka NDC: 64380015202
Lambarka Naadiga: 5501103A, 5501237A, 5501238A, 5501278A, 5501280A, 5501342A, 5501372A, 5501496A, 5501499A, 5501580A, 5501582 5501653A, 5501656A, 5501770A, 5501842A, 5501868A, 5501882A, 5501957A, 5502001A, 5502033A, 5502112 5502115A iyo 5502180A
Taariikhda uu dhacayo: Mar-25, Apr-25, May-25, Jun-25, Jul-25, Agoosto-25, Sep-25, Oct-25, Dec-25, Jan-26, Feb-26, Apr-26, May-26, Jul-26, Aug-26, Oct-26 iyo Nov-26.

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun xun ee ka yimaada isticmaalka dawooyinka dhakhtarku qoray waa in lagu wargeliyaa FDA adigoo booqanaya www.fda.gov/medwatch/report.htm ama wac 1-800-FDA-0178.

On 03/12/2025, Safecor Health, LLC waxay dib u wacday LORAZEPAM 2 MG/ML sababtoo ah Nidaamka Bixinta cilladaysan: Diidashada la arkay ka dib markii xalka afka dib loogu celiyay irbado halbeeg ah. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Heerka II ee dib u yeerista daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: LORAZEPAM 2 MG/ML
Lambarka NDC: 65162068784
Lambarka Naadiga: 24261384 iyo 24370127
Taariikhda uu dhacayo: 03/24/2025 and 04/28/2025

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun xun ee ka yimaada isticmaalka dawooyinka dhakhtarku qoray waa in lagu wargeliyaa FDA adigoo booqanaya www.fda.gov/medwatch/report.htm ama wac 1-800-FDA-0178.

On 03/12/2025, Safecor Health, LLC waxay dib u wacday LORAZEPAM 2 MG/ML sababtoo ah Nidaamka Bixinta cilladaysan: Diidashada la arkay ka dib markii xalka afka dib loogu celiyay irbado halbeeg ah. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Heerka II ee dib u yeerista daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: LORAZEPAM 2 MG/ML
Lambarka NDC: 00121077001
Lambarka Naadiga: 24251067 iyo 24421733
Taariikhda uu dhacayo: 03/25/2025 and 06/03/2025

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun xun ee ka yimaada isticmaalka dawooyinka dhakhtarku qoray waa in lagu wargeliyaa FDA adigoo booqanaya www.fda.gov/medwatch/report.htm ama wac 1-800-FDA-0178.

On 03/12/2025, Safecor Health, LLC waxay dib u wacday LORAZEPAM INTENSOL 2 MG/ML sababtoo ah Nidaamka Bixinta cilladaysan: Diidashada la arkay ka dib markii xal afka ah lagu soo celiyay silinjooyin halbeeg ah. Maamulka Cuntada iyo Dawooyinka ee Maraykanka (FDA) ayaa soo saaray dib u yeedhista heerka II
daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: LORAZEPAM INTENSOL 2 MG/ML
Lambarka NDC: 00054353244
Lambarka Naadiga: 24210274 iyo 24401700
Taariikhda uu dhacayo: 01/31/2025 and 04/25/2025

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun xun ee ka yimaada isticmaalka dawooyinka dhakhtarku qoray waa in lagu wargeliyaa FDA adigoo booqanaya www.fda.gov/medwatch/report.htm ama wac 1-800-FDA-0178.

On 02/26/2025, Alvogen, INC waxay dib u xasuusisay FENTANYL 25 MCG/HR sababtoo ah nidaamka gudbinta cilladaysan - dhejisyadu waxay noqon karaan kuwo isku xiran, midna midba midka kale ku dheggan, hal kiish oo alaabta ah. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Fasalka I ee Xusuusashada
daawooyinka saameeya.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: FENTANYL 25 MCG/HR
Lambarka NDC: 47781042447
Lambarka Naadiga: 108319
Taariikhda uu dhacayo: 04/30/2025

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun xun ee ka yimaada isticmaalka dawooyinka dhakhtarku qoray waa in lagu wargeliyaa FDA adigoo booqanaya https://www.fda.gov/medwatch/report.htm ama wac 1-800-FDA-0178.

On 02/26/2025, Daawooyinka waaweyn ee dib loo soo celiyay LORAZEPAM 0.5 MG sababtoo ah Fashilmay wasakhda/sharciga tilmaamayaasha iyo Dawooyinka Awood-hoosaadka ah: Natiijooyinka aan la cayimin ayaa la helay intii lagu jiray baaritaanka xasilloonida ee Assay iyo Impurities. Cuntada iyo Dawooyinka ee Maraykanka
Maamulka (FDA) ayaa soo saaray dib u soo celinta heerka II ee dawooyinka ay saamaysay.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: LORAZEPAM 0.5 MG
Lambarka NDC: 00904600761
Lambarka Naadiga: N01424, N01425, N01659, N01660, N01668, N01679, N01704, N01745, N01856, N01973 iyo N02079.
Taariikhda uu dhacayo: 03/31/2025, 08/31/2025, 09/2025, 10/31/2025, 02/28/2026, 05/31/2026 and 08/31/2026.

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun xun ee ka yimaada isticmaalka dawooyinka dhakhtarku qoray waa in lagu wargeliyaa FDA adigoo booqanaya www.fda.gov/medwatch/report.htm ama wac 1-800-FDA-0178.

On 02/26/2025, Daawooyinka waaweyn ee dib loo soo celiyay LORAZEPAM 1 MG sababtoo ah Fashilmay wasakhda/sharciga tilmaamayaasha iyo Dawooyinka Awood-hoosaadka ah: Natiijooyinka aan la cayimin ayaa la helay intii lagu jiray baaritaanka xasilloonida ee Assay iyo Impurities. Cuntada iyo Dawooyinka ee Maraykanka
Maamulka (FDA) ayaa soo saaray dib u soo celinta heerka II ee dawooyinka ay saamaysay.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: LORAZEPAM 1 MG
Lambarka NDC: 00904600861
Lambarka Naadiga: N01419, N01420, N01421, N01663, N01664, N01673, N01688, N01747, N01748, N01749, N01792, N01857, N01974 iyo N02081. 
Taariikhda uu dhacayo: 03/31/2025, 06/30/2025, 08/31/2025, 09/30/2025, 08/31/2025, 11/30/2025, 12/31/2025, 02/28/2026, 05/31/2026 and 08/31/2026.

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun xun ee ka yimaada isticmaalka dawooyinka dhakhtarku qoray waa in lagu wargeliyaa FDA adigoo booqanaya www.fda.gov/medwatch/report.htm ama wac 1-800-FDA-0178.

On 1/15/2025, ENDO USA, INC waxay dib u wacday CLONAZEPAM 0.25 MG iyadoo ay ugu wacan tahay Summadaynta: Qaladka Summada ee Awoodda La Shaaciyay; Kartoonada qaar ayaa si khaldan loo calaamadeeyay Xariijimaha finan ka ah gudaha kartoonka alaabta ayaa ka tarjumaya xoogga saxda ah. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray dib u yeerista heerka I ee dawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: CLONAZEPAM 0.25 MG ODT TABLET
Lambarka NDC: 49884030702
Lambarka Naadiga: 550142801, 550142901, 550143001, 550143101, 550143201, 550143301, 550143401, 550147201 IYO 550147401
Taariikhda uu dhacayo: 08 / 31 / 2026.

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun xun ee ka yimaada isticmaalka dawooyinka dhakhtarku qoray waa in lagu wargeliyaa FDA adigoo booqanaya www.fda.gov/medwatch/report.htm ama wac 1-800-FDA-0178.

On 01/15/2025, ENDO USA, INC waxay dib u wacday CLONAZEPAM 1 MG iyadoo ay ugu wacan tahay Summadaynta: Qaladka Summada ee Awoodda La Shaaciyay; Kartoonada qaar ayaa si khaldan loo calaamadeeyay Xariijimaha finan ka ah gudaha kartoonka alaabta ayaa ka tarjumaya xoogga saxda ah. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray dib u yeerista heerka I ee dawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: CLONAZEPAM 1 MG ODT TABLET
Lambarka NDC: 49884030902
Lambarka Naadiga: 550145201, 550175901, 550176001 IYO 550176201
Taariikhda uu dhacayo: 08/31/2026 AND 02/28/2027

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun xun ee ka yimaada isticmaalka dawooyinka dhakhtarku qoray waa in lagu wargeliyaa FDA adigoo booqanaya www.fda.gov/medwatch/report.htm ama wac 1-800-FDA-0178.

On 1/15/2025, ENDO USA, INC waxay dib u wacday CLONAZEPAM 2 MG iyadoo ay ugu wacan tahay Summadaynta: Qaladka Summada ee Awoodda La Shaaciyay; Kartoonada qaar ayaa si khaldan loo calaamadeeyay Xariijimaha finan ka ah gudaha kartoonka alaabta ayaa ka tarjumaya xoogga saxda ah. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray dib u yeerista heerka I ee dawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: CLONAZEPAM 2 MG ODT TABLET
Lambarka NDC: 49884031002
Lambarka Naadiga: 550176501 IYO 550176601
Taariikhda uu dhacayo: 02/28/2027

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun xun ee ka yimaada isticmaalka dawooyinka dhakhtarku qoray waa in lagu wargeliyaa FDA adigoo booqanaya https://www.fda.gov/medwatch/report.htm ama wac 1-800-FDA-0178.

On 01/08/2025, Lupine Pharmaceuticals waxay dib u soo celisay LEVOTHYROXINE SODIUM 75 MCG sababtoo ah Najaasaha Fashilmay / Tilmaamaha Waxyeelaynta: Natiijooyinka qeexan ee ka baxsan ee lagu arkay walaxda daroogada ee baaritaanka wasakhnimada muddada 3-bilood ee daraasadda xasilloonida muddada dheer. Cuntada iyo Dawooyinka ee Maraykanka 
Maamulka (FDA) ayaa soo saaray dib u soo celinta heerka II ee dawooyinka ay saamaysay.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: LEVOTHYROXINE SODIUM 75 MCG
Lambarka NDC: 68180096703
Lambarka Naadiga: LA01276
Taariikhda uu dhacayo: 07/2026

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya https://www.fda.gov/medwatch/report.htm ama wacaya 1-800-FDA-0178.

On 12/25/2024, MACLEODS PHARMACUTICALS waxay dib u soo celisay OLANZAPINE 2.5 MG sababtoo ah Tilmaamaha Waxyeelada/Degradation-ka ee Fashilmay. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Heerka II ee dib u yeerista daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: OLANZAPINE 2.5 MG TABLET
Lambarka NDC: 33342006707
Lambarka Naadiga: BOB12318A
Taariikhda uu dhacayo: 07/31/2027

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun xun ee ka yimaada isticmaalka dawooyinka dhakhtarku qoray waa in lagu wargeliyaa FDA adigoo booqanaya www.fda.gov/medwatch/report.htm ama wac 1-800-FDA-0178.

On 12/18/2024, Soo saaraha Viatris ee Mylan wuxuu dib u soo celiyay LEVOTHYROXINE SODIUM 25 MCG sababtoo ah Dawooyinka Sare iyo Awood-hoosaadka: Guuldarrooyinka awoodda ee la helay. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Heerka II ee dib u yeerista daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: LEVOTHYROXINE SODIUM 25 MCG
Lambarka NDC: 00378180010 iyo 00378180077
Lambarka Naadiga: 8181875, 8174497, 3209099, 3206534, 3196137
Taariikhda uu dhacayo: 8/2025, 4/2025, 10/2025, 8/2025 iyo 4/2025

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun xun ee ka yimaada isticmaalka dawooyinka dhakhtarku qoray waa in lagu wargeliyaa FDA adigoo booqanaya www.fda.gov/medwatch/report.htm ama wac 1-800-FDA-0178.

On 12/18/2024, Soo saaraha Viatris ee Mylan wuxuu dib u soo celiyay LEVOTHYROXINE SODIUM 50 MCG sababtoo ah Dawooyinka Sare iyo Awood-hoosaadka: Guuldarrooyinka awoodda ee la helay. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Heerka II ee dib u yeerista daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: LEVOTHYROXINE SODIUM 50 MCG
Lambarka NDC: 00378180310 iyo 00378180377
Lambarka Naadiga: 8174701, 8182228, 3193984 iyo 3206790
Taariikhda uu dhacayo: 4/2025, 8/2025, 3/2025 iyo 8/2025

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun xun ee ka yimaada isticmaalka dawooyinka dhakhtarku qoray waa in lagu wargeliyaa FDA adigoo booqanaya www.fda.gov/medwatch/report.htm ama wac 1-800-FDA-0178.

On 12/18/2024, Soo saaraha Viatris ee Mylan wuxuu dib u soo celiyay LEVOTHYROXINE SODIUM 75 MCG sababtoo ah Dawooyinka Sare iyo Awood-hoosaadka: Guuldarrooyinka awoodda ee la helay. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Heerka II ee dib u yeerista daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: LEVOTHYROXINE SODIUM 75 MCG
Lambarka NDC: 00378180577 iyo 00378180510
Lambarka Naadiga: 8177078, 8168596, 3199313, 3194118, 3186238, 3209590, 3199317 iyo 3188733
Taariikhda uu dhacayo: 5/2025, 1/2025, 5/2025, 3/2025, 12/2024, 10/2025, 5/2025 iyo 1/2025

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun xun ee ka yimaada isticmaalka dawooyinka dhakhtarku qoray waa in lagu wargeliyaa FDA adigoo booqanaya www.fda.gov/medwatch/report.htm ama wac 1-800-FDA-0178.

On 12/18/2024, Soo saaraha Viatris ee Mylan wuxuu dib u soo celiyay LEVOTHYROXINE SODIUM 88 MCG sababtoo ah Dawooyinka Sare iyo Awood-hoosaadka: Guuldarrooyinka awoodda ee la helay. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Heerka II ee dib u yeerista daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: LEVOTHYROXINE SODIUM 88 MCG
Lambarka NDC: 00378180777 iyo 00378180710
Lambarka Naadiga: 8180781, 3191628, 3197139, 3188976, 3184929, iyo 3204909
Taariikhda uu dhacayo: 8/2025, 2/2025, 4/2025, 1/2025, 12/2024 iyo 8/20

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun xun ee ka yimaada isticmaalka dawooyinka dhakhtarku qoray waa in lagu wargeliyaa FDA adigoo booqanaya www.fda.gov/medwatch/report.htm ama wac 1-800-FDA-0178.

On 12/18/2024, Soo saaraha Viatris ee Mylan wuxuu dib u soo celiyay LEVOTHYROXINE SODIUM 100 MCG sababtoo ah Dawooyinka Awoodda Sare leh iyo Daawada Subpotent: guuldarrooyin awoodeed oo la helay. Maraykanka

Maamulka Cuntada iyo Dawooyinka (FDA) ayaa soo saaray Heerka II ee dib u soo celinta daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: LEVOTHYROXINE SODIUM 100 MCG
Lambarka NDC: 00378180977 iyo 00378180910
Lambarka Naadiga: 8171269, 8179579, 3183815, 3189147,3192027, 3202894, 3192026, 3199781, 3192028 iyo 3202895
Taariikhda uu dhacayo: 2/2025, 7/2025, 11/2024, 1/2025, 2/2025, 7/2025, 2/2025, 6/2025, 2/2025 iyo 7/2025

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun xun ee ka yimaada isticmaalka dawooyinka dhakhtarku qoray waa in lagu wargeliyaa FDA adigoo booqanaya www.fda.gov/medwatch/report.htm ama wac 1-800-FDA-0178.

On 12/18/2024, Soo saaraha Viatris ee Mylan wuxuu dib u soo celiyay LEVOTHYROXINE SODIUM 112 MCG sababtoo ah Dawooyinka Awoodda Sare leh iyo Daawada Subpotent: guuldarrooyin awoodeed oo la helay. Maraykanka

Maamulka Cuntada iyo Dawooyinka (FDA) ayaa soo saaray Heerka II ee dib u soo celinta daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: LEVOTHYROXINE SODIUM 112 MCG
Lambarka NDC: 00378181177 iyo 00378181110
Lambarka Naadiga: 8171623, 8164486, 3205462, 3192428 iyo 3184096
Taariikhda uu dhacayo: 2/2025, 11/2024, 8/2025, 2/2025 iyo 11/2024

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun xun ee ka yimaada isticmaalka dawooyinka dhakhtarku qoray waa in lagu wargeliyaa FDA adigoo booqanaya www.fda.gov/medwatch/report.htm ama wac 1-800-FDA-0178.

On 12/18/2024, Soo saaraha Viatris ee Mylan wuxuu dib u soo celiyay LEVOTHYROXINE SODIUM 125 MCG sababtoo ah Dawooyinka Awoodda Sare leh iyo Daawada Subpotent: guuldarrooyin awoodeed oo la helay. Maraykanka

Maamulka Cuntada iyo Dawooyinka (FDA) ayaa soo saaray Heerka II ee dib u soo celinta daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: LEVOTHYROXINE SODIUM 125 MCG
Lambarka NDC: 00378181377 iyo 00378181310
Lambarka Naadiga: 3182797, 8177587 iyo 3199816
Taariikhda uu dhacayo: 11 / 2024 iyo 6 / 2025

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun xun ee ka yimaada isticmaalka dawooyinka dhakhtarku qoray waa in lagu wargeliyaa FDA adigoo booqanaya www.fda.gov/medwatch/report.htm ama wac 1-800-FDA-0178.

On 12/18/2024, Soo saaraha Viatris ee Mylan wuxuu dib u soo celiyay LEVOTHYROXINE SODIUM 137 MCG sababtoo ah Dawooyinka Awoodda Sare leh iyo Daawada Subpotent: guuldarrooyin awoodeed oo la helay. Maraykanka

Maamulka Cuntada iyo Dawooyinka (FDA) ayaa soo saaray Heerka II ee dib u soo celinta daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: LEVOTHYROXINE SODIUM 137 MCG
Lambarka NDC: 00378182377 iyo 00378182310
Lambarka Naadiga: 8165919, 8172050, 8183251, 3185542, 3192838 iyo 3208172
Taariikhda uu dhacayo: 12/2024, 3/2025, 9/2025, 12/2024, 3/2025 iyo 10/2025

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun xun ee ka yimaada isticmaalka dawooyinka dhakhtarku qoray waa in lagu wargeliyaa FDA adigoo booqanaya www.fda.gov/medwatch/report.htm ama wac 1-800-FDA-0178.

On 12/18/2024, Soo saaraha Viatris ee Mylan wuxuu dib u soo celiyay LEVOTHYROXINE SODIUM 150 MCG sababtoo ah Dawooyinka Sare iyo Awood-hoosaadka: Guuldarrooyinka awoodda ee la helay. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Heerka II ee dib u yeerista daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u yeerista waa: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: LEVOTHYROXINE SODIUM 150 MCG
Lambarka NDC: 00378181577 iyo 00378181510
Lambarka Naadiga: 8177720 iyo 3200218
Taariikhda uu dhacayo: 6 / 2025 iyo 6 / 2025

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun xun ee ka yimaada isticmaalka dawooyinka dhakhtarku qoray waa in lagu wargeliyaa FDA adigoo booqanaya www.fda.gov/medwatch/report.htm ama wac 1-800-FDA-0178.

On 12/18/2024, Soo saaraha Viatris ee Mylan wuxuu dib u soo celiyay LEVOTHYROXINE SODIUM 175 MCG sababtoo ah Dawooyinka Sare iyo Awood-hoosaadka: Guuldarrooyinka awoodda ee la helay. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Heerka II ee dib u yeerista daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u yeerista waa: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: LEVOTHYROXINE SODIUM 175 MCG
Lambarka NDC: 00378181777 iyo 00378181710
Lambarka Naadiga: 3192915, 8172108 iyo 3208680
Taariikhda uu dhacayo: 3 / 2025 iyo 9 / 2025

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun xun ee ka yimaada isticmaalka dawooyinka dhakhtarku qoray waa in lagu wargeliyaa FDA adigoo booqanaya www.fda.gov/medwatch/report.htm ama wac 1-800-FDA-0178.

On 12/18/2024, Soo saaraha Viatris ee Mylan wuxuu dib u soo celiyay LEVOTHYROXINE SODIUM 200 MCG sababtoo ah Dawooyinka Sare iyo Awood-hoosaadka: Guuldarrooyinka awoodda ee la helay. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Heerka II ee dib u yeerista daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: LEVOTHYROXINE SODIUM 200 MCG
Lambarka NDC: 00378181977 iyo 00378181910
Lambarka Naadiga: 8179847 iyo 3203518
Taariikhda uu dhacayo: 7 / 2025 iyo 7 / 2025

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun xun ee ka yimaada isticmaalka dawooyinka dhakhtarku qoray waa in lagu wargeliyaa FDA adigoo booqanaya www.fda.gov/medwatch/report.htm ama wac 1-800-FDA-0178.

On 12/11/2024, Accord Healthcare Inc waxay dib u wacday LEVOTHYROXINE SODIUM 75 MCG iyadoo ay ugu wacan tahay daroogo hoosaysa. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Heerka II ee dib u yeerista daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: LEVOTHYROXINE SODIUM 75 MCG
Lambarka NDC: 16729044917
Lambarka Naadiga: D2300191
Taariikhda uu dhacayo: 12/31/2025

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacayo 1-800-FDA-0178.

On 12/11/2024, Shirkadda Lannett Inc. waxay dib u wacday LISDEXAMFETAMINE DIMESYLATE 10 MG sababtoo ah Fashilmay Tilmaamaha Midaysanaanta Mawduuca: Alaabtu waxay ku guuldareysatay inay la kulanto xaddidaadda waxqabadka ee isku midka ahaanshaha nuxurka. Maamulka Cuntada iyo Dawooyinka ee Maraykanka (FDA) ayaa soo saaray a 
Fasalka II Dib u soo celinta daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: LISDEXAMFETAMINE DIMESYLATE 10 MG
Lambarka NDC: 00527466137
Lambarka Naadiga: 23274856A
Taariikhda uu dhacayo: 04/30/2025

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun xun ee ka yimaada isticmaalka dawooyinka dhakhtarku qoray waa in lagu wargeliyaa FDA adigoo booqanaya www.fda.gov/medwatch/report.htm ama wac 1-800-FDA-0178.

On 11/20/2024, Legacy Pharmace dib loo wacay LISINOPRIL 10 MG iyadoo ay ugu wacan tahay joogitaanka shay shisheeye: Farmashiistaha ayaa helay jajab bir ah oo ku dhex jira kiniinka lisinopril 10 mg. Maamulka Cuntada iyo Dawooyinka ee Maraykanka (FDA) ayaa soo saaray a Soocelinta Heerka II daawooyinka ay saameysay.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: LISINOPRIL 10 MG
Lambarka NDC: 68645061090
Lambarka Naadiga: 241103
Taariikhda uu dhacayo: 5/31/2026

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya https://www.fda.gov/medwatch/report.htm ama wacayo 1-800-FDA-0178.

On 11/06/2024, Accord Healthcare dib loo wacay CINACALCET HCL 30 MG sababtoo ah Fashilmay Najaasaha/Degration Specifications: joogitaanka nitrosamine wasakh ah, N-nitrosocinacalcet, ka sarreeya xadka qaadashada maalin kasta la aqbali karo (ADI). Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Heerka II ee dib u yeerista daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: CINACALCET HCL 30 MG
Lambarka NDC: 16729044015
Lambarka Naadiga: MM2212869, M2216362 iyo M2215969
Taariikhda uu dhacayo: 08/2025, 09/2025 iyo 10/2025

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun xun ee ka yimaada isticmaalka dawooyinka dhakhtarku qoray waa in lagu wargeliyaa FDA adigoo booqanaya www.fda.gov/medwatch/report.htm ama wac 1-800-FDA-0178.

On 10/23/2024, Bionpharma dib u wacday ATOVAQUONE 750 MG/5ML sababtoo ah Wasakhda Microbial ee Alaabada Aan nadiifka ahayn: Alaabta waxaa la ogaaday inay ku wasakhowday bakteeriyada Cohnella. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray dib u yeerista heerka I ee dawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: ATOVAQUONE 750 MG/5ML
Lambarka NDC: 69452025287
Lambarka Naadiga: 2310083
Taariikhda uu dhacayo: 09/30/2025

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun xun ee ka yimaada isticmaalka dawooyinka dhakhtarku qoray waa in lagu wargeliyaa FDA adigoo booqanaya www.fda.gov/medwatch/report.htm ama wac 1-800-FDA-0178.

On 10/23/2024, Breckenridge waxa uu dib u wacay DULOXETINE HCL 20 MG sababtuna tahay Kala leexashada CGMP: Joogitaanka Nitrosamine ee Walaxda La Xidhiidha Maandooriyaha (NDSRI), N-nitroso-duloxetine, oo ka sarreeya xadka ku meel gaarka ah ee la soo jeediyay. Maamulka Cuntada iyo Dawooyinka ee Maraykanka (FDA) ayaa soo saaray a
Fasalka II Dib u soo celinta daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: DULOXETINE HCL 20 MG
Lambarka NDC: 51991074605
Lambarka Naadiga: 220128
Taariikhda uu dhacayo: 12/2024

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun xun ee ka yimaada isticmaalka dawooyinka dhakhtarku qoray waa in lagu wargeliyaa FDA adigoo booqanaya www.fda.gov/medwatch/report.htm ama wac 1-800-FDA-0178.

09/04/2024, Dr. 
Qeexitaannada wasakhda/xumaynta: Natiijooyinka wasakhda aan la garanayn, waxay ahaayeen 0.13% iyo 0.11% siday u kala horreeyaan, oo dhaaftay 0.10% xadka qeexitaanka. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Heerka II ee dib u yeerista daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: IBUPROFEN 400 MG
Lambarka NDC: 55111068201 iyo 55111068205
Nambarka (tirada): C2207529, C2210993, C2207530, C2210992, C2210994, C2213304 iyo C2213305
Taariikhda (yada) uu Dhacayo: 5/31/2026, 9/30/2026, 5/31/2026, 9/30/2026 AND 11/30/2026

Waxa ay tahay inaad sameyso:

• Ha sii wadin isticmaalka IBUPROFEN 400 MG haddii dib loo soo celiyay
• Hubi summadaada dawada si aad u aragto haddii aad leedahay wax IBU ah oo ku jira lambarada tirada badan ee ay saamaysay iyo taariikhda dhicitaanka.
• Haddii aad haysatid daawada, la xidhiidh farmashiyaha aad ka heshay. Dhacdooyinka xun xun ee ka yimaada isticmaalka dawooyinka dhakhtarku qoray waa in lagu wargeliyaa FDA adigoo booqanaya www.fda.gov/medwatch/report.htm ama wac 1-800-FDA-0178.

Markay ahayd 09/04/2024, Dr. Ready's dib loogu yeedhay IBUPROFEN 600 MG sababtuna tahay qeexida wasakhda fashilantay/xumaynta: natiijooyinka wasakhda aan la garanayn, waxay ahaayeen 0.13% iyo 0.11% siday u kala horreeyaan, oo dhaaftay 0.10% xadka qeexitaanka. Maamulka Cuntada iyo Dawooyinka ee Maraykanka
(FDA) ayaa soo saartay Dib-u-celinta Heerka II ee dawooyinka ay saamaysay.

Macluumaad dheeri ah oo ku saabsan dib u yeerinta waa: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: IBUPROFEN 600 MG
Lambarka NDC: 55111068301 IYO 55111068305
Nambarka (tirada): C2207527, C2210864, ​​C2213018, C2207528, C2210860, C2213016, C2213017, C2301852, C2302056 IYO C230257
Taariikhda (s): 5/31/2026, 9/30/2026, 11/30/2026, 5/31/2026, 9/30/2026,11/30/2026 AND 1/31/2024

Waxa ay tahay inaad sameyso:

• Ha sii wadin isticmaalka IBUPROFEN 600 MG haddii dib loo soo celiyay
• Hubi summadaada dawada si aad u aragto haddii aad leedahay wax IBU ah oo ku jira lambarada tirada badan ee ay saamaysay iyo taariikhda dhicitaanka.
• Haddii aad haysatid daawada, la xidhiidh farmashiyaha aad ka heshay. Dhacdooyinka xun xun ee ka yimaada isticmaalka dawooyinka dhakhtarku qoray waa in lagu wargeliyaa FDA adigoo booqanaya www.fda.gov/medwatch/report.htm ama wac 1-800-FDA-0178.

On 08/07/2024, Glenmark Pharmaceuticals waxay dib u wacday AZELAIC ACID 15 % leexashada CGMP awgeed. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Heerka II ee dib u yeerista daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: AZELAIC ACIID 15 % GEL
Lambarka NDC: 68462062652
Lambarka Naadiga: 19241453
Taariikhda uu dhacayo: 03/31/2026

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacayo 1-800-FDA-0178.

On 08/07/2024, Amerisource Adeegyada Caafimaadka waxa dib loogu yeedhay POTASSIUM KHLORIDE 10 MEQ sababtuna tahay qeexitaannada kala diris ee fashilmay. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray dib u yeerista heerka I ee dawooyinka ay saameeyeen.
Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: Potassium chloride 10 MEQ
Lambarka NDC: 68001039603

Sababtoo ah tirada badan ee tirada badan ee ay saamaysay, fadlan tixraac bogga internetka ee FDA ee kor ku xusan si aad u hesho macluumaad gaar ah oo ku saabsan tirada badan ee la xidhiidha daawadaada

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacayo 1-800-FDA-0178.

On 08/07/2024, Endo Pharmaceuticals waxay dib u wacday CLONAZEPAM 0.125 MG sababtoo ah cilad calaamadeysan oo ku saabsan xoogga la sheegay; Kartoonada qaar ayaa si khaldan loogu calaamadeeyay 0.125 mg halkii 0.25 mg. Xariijimaha finan ka ah gudaha kartoonada alaabta ayaa ka tarjumaysa xoogga saxda ah ee 0.25 mg. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray dib u yeerista heerka I ee dawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: CLONAZEPAM 0.125 MG ODT
Lambarka NDC: 49884030602
Lambarka Naadiga: 550147301
Taariikhda uu dhacayo: 08/31/2026

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacayo 1-800-FDA-0178.

PRAVASTATIN SODIUM 80 MG

Markay ahayd 7/24/2024, GLENMARK PHARMAC waxay dib u wacday PRAVASTATIN SODIUM 80 MG sababtuna tahay Tilmaamaha Falalka Fashilan: Natiijooyinka hoosta faahfaahinta. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Heerka II ee dib u yeerista daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: PRAVASTATIN SODIUM 80 MG
Lambarka NDC: 68462019890
Lambarka Naadiga: 17211249, 17211264, 17211266,17211286, 17211525, 17211535, 17211549, 17211787, 17211801, 17212041 17212088, 17212106, 17212346, 17212345, 17220053, 17220054, 17220055 iyo 17220309
Taariikhda uu dhacayo: 6/30/2024, 7/31/2024, 8/31/2024, 9/30/2024, 10/31/2024, 12/31/2024 and 1/31/2025

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacayo 1-800-FDA-0178.

FLUDROCORTISONE ACETATE 0.1 MG

Markay ahayd 7/24/2024, TEVA PHARMA waxay dib u wacday FLUDROCORTISONE ACETATE 0.1 MG iyadoo ay ugu wacan tahay waxyaalaha wasakhda/jarida ah ee fashilantay: Badeecada waxaa dib loogu yeeraa maaddooyinka API-ga laxiriira iyo wasakh aan la aqoon oo ka sarreeya xadka qeexida. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Heerka II ee dib u yeerista daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: FLUDROCORTISONE ACETATE 0.1 MG
Lambarka NDC: 00555099702
Lambarka Naadiga: CNSDH, CNWVM, CNWWH, CNXKW, CNXKY, CNXMB, CNXMH, CPBTP iyo CPBTV
Taariikhda uu dhacayo: 6/30/2024, 7/31/2024, 9/30/2024 and 11/30/2024

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
•  Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacayo 1-800-FDA-0178

Potassium chloride 10 MEQ

On 07/24/2024 Glenmark Pharmaceuticals waxay dib u wacday POTASSIUM KHLORIDE 10 MEQ sababtoo ah qeexitaannada kala diris ee fashilmay Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay dib u soo celinta heerka I ee dawooyinka ay saameysay.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: Potassium chloride 10 MEQ
Lambarka NDC: 68462035705
Nambarka (tirada): 17221197, 17221386, 17221385, 17221489, 17221504, 17221530, 17221561, 17221579, 17221568, 17221702 17221704, 17221898, 17221993, 17222029, 17222300, 17222304, 17222278, 17222609, 17222395 iyo 17222589 
Taariikhda (yada) uu Dhacayo: 5/31/2024, 6/30/2024, 7/31/2024, 8/31/2024, 10/31/2024 and 11/30/2024

Waxa ay tahay inaad sameyso:

• Ha sii wadin isticmaalka POTASSIUM KHLORIDE 10 MEQ haddii dib loo soo celiyay
• Hubi summadaada daawada laguu qoray si aad u aragto haddii aad leedahay wax POTASSIUM KHLORIDE ah oo ku jira lambarada tirada la saameeyey iyo taariikhda dhicitaanka.
• Haddii aad qaadatay daawada, la xiriir farmasiga aad ka heshay. Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacayo 1-800-FDA-0178.

Potassium chloride 10 MEQ

On 07/24/2024 Glenmark Pharmaceuticals waxay dib u wacday POTASSIUM KHLORIDE 10 MEQ sababtoo ah qeexitaannada kala diris ee fashilmay Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay dib u soo celinta heerka I ee dawooyinka ay saameysay.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: Potassium chloride 10 MEQ
Lambarka NDC: 68462035701
Nambarka (tirada): 17221446, 17221445, 17221393, 17221403, 17221405, 17221503, 17221508, 17221567, 17221566, 17221719, 17221731, 17221891, 17221892, 17221900 17221992, 17222022, 17222056, 17222043, 17222068, 17222079, 17222099, 17222103, 17222114, 17222119 17222188, 17222199, 17222209, 17222200, 17222265, 17222269, 17222527, 17222530, 17222583, 17222586
Taariikhda (s): 5/31/2024, 6/30/2024, 7/31/2024, 8/31/2024, 9/30/2024, 10/31/2024, and 11/30/2024

Waxa ay tahay inaad sameyso:

• Ha sii wadin isticmaalka POTASSIUM KHLORIDE 10 MEQ haddii dib loo soo celiyay
• Hubi summadaada daawada laguu qoray si aad u aragto haddii aad leedahay wax POTASSIUM KHLORIDE ah oo ku jira lambarada tirada la saameeyey iyo taariikhda dhicitaanka.
• Haddii aad qaadatay daawada, la xiriir farmasiga aad ka heshay. Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacayo 1-800-FDA-0178.

AMOXICILLIN-CLAVULANATE POTASS 400-57MG CHEWABLE

Taariikhdu markay ahayd 6/26/2024, TEVA PHARMACEUTICALS waxay dib u wacday AMOXICILLIN-CLAVULANATE POTASS 400-57MG taas oo ay ugu wacan tahay daroogo hoosaysa. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Heerka II ee dib u yeerista daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: AMOXICILLIN-CLAVULANATE BOTASS 400-57MG NDC Number: 00093227234 Lot Number: 100047634 iyo 35449379A
Taariikhda uu dhacayo: 04 / 2025 iyo 7 / 2024

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacayo 1-800-FDA-0178.

DULOXETINE HCL 60 MG

Markay ahayd 6/26/2024, Breckenridge Pharmaceutical ayaa dib u wacday DULOXETINE HCL 60 MG iyadoo ay ugu wacan tahay leexleexyada CGMP: Joogitaanka Nitrosamine Walxaha La Xiriira wasakhnimada (NDSRI), N-nitroso-duloxetine, oo ka sarreysa xadka ku meel gaarka ah ee la soo jeediyay. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Heerka II ee dib u yeerista daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: DULOXETINE HCL 60 MG NDC Number: 51991074890 Lot Number: 230035C iyo 230101C
Taariikhda uu dhacayo: 11/30/2025 and 12/31/2025

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacayo 1-800-FDA-0178.

METHYLPHENIDATE ER 36 MG

Markay ahayd 07/10/2024, Trigen Laboratories waxay dib u wacday METHYLPHENIDATE ER 36 MG sababtoo ah qeexitaannada kala dirid ee guuldareystay: alaabtan waa la soo celiyay sababtoo ah dufcadan oo aan buuxin shuruudaha kala dirida. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Heerka II ee dib u yeerista daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: METHYLPHENIDATE ER 36 MG NDC Nambarka: 13811070810 Lambarka Lot: 230159M
Taariikhda uu dhacayo: 02/28/2026

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacayo 1-800-FDA-0178.

METOPROLOL TARTRATE 25 MG

Markay ahayd 06/05/2024, Rubicon Research Private Limited waxay dib u wacday METOPROLOL TARTRATE 25 MG sababtoo ah joogitaanka walax shisheeye: Birta kiniinka ku jirta. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Heerka II ee dib u yeerista daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: METOPROLOL TARTRATE 25 MG NDC Number: 52817036000 Lot Number: 231037H1
Taariikhda uu dhacayo: 06/2027

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacayo 1-800-FDA-0178.

PHENAZOPYRIDINE HCL 100 MG

Markay ahayd 06/19/2024, Shaybaarada Winder waxay dib u waceen PHENAZOPYRIDINE HCL 100 MG isku darka alaabta awgeed. Dhalada kaniiniga ah ee Phenazopyridine 100mg waxa ku jira kaniini Phenobarbital 16.2mg. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Heerka II ee dib u yeerista daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dib loo celiyay Dawada: PHENAZOPYRIDINE HCL 100 MG NDC Nambarka: 75826011410 Lambarka Lot: 1142404

Taariikhda uu dhacayo: 02/27/2027

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacayo 1-800-FDA-0178.

RIZATRIPTAN 5 MG

Markay ahayd 06/12/2024, Glemark Pharmaceuticals waxay dib u wacday RIZATRIPTAN 5 MG sababtoo ah natiijooyinka wasakhda ah ee ka sarreeya xadka la aqbali karo ee FDA. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Heerka II ee dib u yeerista daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:
Dib loo celiyay Dawada: RIZATRIPTAN 5 MG NDC Number: 68462046599 Lot Number: 19233788 iyo 19224445

Taariikhda uu dhacayo: 09/2025 iyo 09/2024

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacayo 1-800-FDA-0178.

RIZATRIPTAN 10 MG

Markay ahayd 06/12/2024, Glemark Pharmaceuticals waxay dib u wacday RIZATRIPTAN 10 MG sababtoo ah natiijooyinka wasakhda ah ee ka sarreeya xadka la aqbali karo ee FDA. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Heerka II ee dib u yeerista daawooyinka ay saameeyeen.
Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:
Dib loo celiyay Dawada: RIZATRIPTAN 10 MG NDC Number: 68462046699 Lot Number: 19224217, 19233789 iyo 19224444

Taariikhda uu dhacayo: 09/2024, 09/2025 iyo 09/2024

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacayo 1-800-FDA-0178.

RIZATRIPTAN ODT 10 MG

Markay ahayd 06/12/2024, Glemark Pharmaceuticals waxay dib u wacday RIZATRIPTAN ODT 10 MG sababtoo ah natiijooyinka wasakhda ah ee ka sarreeya xadka la aqbali karo ee FDA. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Heerka II ee dib u yeerista daawooyinka ay saameeyeen.
Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:
Dawada la xasuusto: RIZATRIPTAN ODT 10 MG NDC Number: 68462046806 Lot Number: 19223402, 19224858 iyo 19232492
Taariikhda uu dhacayo: 07/2024, 11/2024 iyo 6/2025

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacayo 1-800-FDA-0178.

LOSARTAN POTASSIUM 25 MG

07/12/2023 STRIDES PHARMA waxay dib u wacday LOSARTAN POTASSIUM 25 MG sababtoo ah joogitaanka walxo shisheeye Fasalka II Xusuuso daawooyinka ay saameysay.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: http://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: LOSARTAN POTASSIUM 25 MG
Lambarka NDC: 64380093308
Lambarka Naadiga: 7901903A
Taariikhda uu dhacayo: 04/30/2024

 Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya fda.gov/medwatch/report.htm ama wacayo 1-800-FDA-0178.

INSULIN GLARGINE-YFGN 100/ML

Maajo 4, 2022, MYLAN SPECIALTY waxay dib u wacday INSULIN GLARGINE-YFGN 100/ML sababtoo ah calaamadinta ka maqan fijaanadda. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray dib u yeerista heerka I ee dawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: http://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

• Dawada la xasuusto: INSULIN GLARGINE-YFGN 100/ML
• Lambarka NDC: 49502039380
• Lambarka (tirada): BF21002800
• Taariikhda (yada) uu Dhacayo: 8/2023

Waxa ay tahay inaad sameyso:

• Ha sii wadin isticmaalka INSULIN GLARGINE-YFGN 100/ML haddii dib loo soo celiyay
• Hubi summadaada dawada laguu qoray si aad u aragto haddii aad leedahay wax INSULIN GLARGINE-YFGN ah oo ku jira lambarada tirada la saameeyey iyo taariikhda dhicitaanka.
• Haddii aad qaadatay daawada, la xiriir farmasiga aad ka heshay. Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacaya 1-800-FDA-0178.

HUMALOG 100/ML

Maajo 25, 2022, CAAFIMAADKA CARDINAL wuxuu dib u wacay HUMALOG 100/ML sababtoo ah soo-gaadhista heerkul aad u daran. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray dib u yeerista heerka I ee dawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: http://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

• Dawada la xasuusto: HUMALOG 100/ML
• Lambarka NDC: 00002751659
• Nambarka (tirada): AAN LA GARAN
• Taariikhda (yada) uu Dhacayo: AAN LA GARAN

Waxa ay tahay inaad sameyso:

• Ha sii wadin isticmaalka HUMALOG 100/ML haddii dib loo soo celiyay
• Hubi summadaada dawada laguu qoray si aad u aragto haddii aad hayso wax HUMALOG ah oo ku jira lambarada tirada la saameeyey iyo taariikhda dhicitaanka.
• Haddii aad qaadatay daawada, la xiriir farmasiga aad ka heshay. Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacaya 1-800-FDA-0178.

GUDUBKA 0.004 %

Abriil 13, 2022, MYLAN waxay dib u soo celisay TRAVOPROST 0.004 % iyadoo ay ugu wacan tahay joogitaanka wasakh. Maamulka Cuntada iyo Dawooyinka ee Maraykanka (FDA) ayaa soo saaray a Soocelinta Heerka II oo ka mid ah
daawooyinka saameeya.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: http://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

• Dawada la xasuusto: GUDUBKA 0.004 %
• Lambarka NDC: 00378965132
• Nambarka (tirada): TV11W101
• Taariikhda (yada) uu Dhacayo: Mar 2023

Waxa ay tahay inaad sameyso:

• Ha sii wadin isticmaalka TRAVOPROST 0.004 % haddii dib loo soo celiyay
• Hubi summadaada dawada laguu qoray si aad u aragto haddii aad leedahay wax MUQAAL ah oo ku jira lambarada tirada la saameeyey iyo taariikhda dhicitaanka.
• Haddii aad qaadatay daawada, la xiriir farmasiga aad ka heshay. Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacayo 1-800-FDA-0178.

GLYCOPYRRATE 1 MG

Abriil 6, 2022, AUROBINDO PHARMA waxay dib u wacday GLYCOPYRROLATE 1 MG iyadoo ay ugu wacan tahay joogitaanka wasakh. Maamulka Cuntada iyo Dawooyinka ee Maraykanka (FDA) ayaa soo saaray a Soocelinta Heerka II daawooyinka ay saameysay.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: http://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

• Dawada la xasuusto: GLYCOPYRRATE 1 MG
• Lambarka NDC: 13107001401
• Nambarka (tirada): 01421008A1
• Taariikhda (yada) uu Dhacayo: 03/2023

Waxa ay tahay inaad sameyso:

• Ha sii wadin isticmaalka GLYCOPYRROLATE 1 MG haddii dib loo soo celiyay
• Hubi summadaada dawada laguu qoray si aad u aragto haddii aad leedahay wax GLYCOPYRROLATE ee nambarada saamiga la saameeyey iyo taariikhaha dhacayo.
• Haddii aad qaadatay daawada, la xiriir farmasiga aad ka heshay. Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacayo 1-800-FDA-0178.

SYMJEPI 0.3MG/0.3

Abriil 13, 2022, USWM, LLC, DB waxay dib u wacday SYMJEPI 0.3MG/0.3 sababtoo ah suurtagalnimada in nidaamka gaarsiinta uu cilladaysan yahay. Maamulka Cuntada iyo Dawooyinka ee Maraykanka (FDA) ayaa soo saaray a Fasalka I Xusuusta daawooyinka ay saameysay.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: http://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

• Dawada la xasuusto: SYMJEPI 0.3MG/0.3
• Lambarka NDC: 78670013002
• Lambarka Naadiga: 21041W, 21081W, 21102W
• Taariikhda uu dhacayo: 8/31/2022, 11/30/2022, 2/8/2023

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacayo 1-800-FDA-0178.

FIRVANQ 50 MG/ML

Oktoobar 13, 2021, AZURITY PHARMACEUTICALS, INC waxay dib u wacday FIRVANQ 50 MG/ML isku darka alaabta awgeed. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray dib u yeerista heerka I ee dawooyinka ay saameeyeen.
Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: http://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

• Dawada la xasuusto: FIRVANQ 50 MG/ML
• Lambarka NDC: 65628020605
• Nambarka (tirada): 21035
• Taariikhda (yada) uu Dhacayo: July 31, 2022

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacaya 1-800-FDA-0178.

Qalabka degdegga ah ee GLUCAGON 1 MG

Oktoobar 20, 2021, ELI LILLY & CO. waxay dib u soo celiyeen qalabka degdegga ah ee GLUCAGON KIT 1 MG awood-hoosaad awgeed. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray dib u yeerista heerka I ee dawooyinka ay saameeyeen.
Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: http://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

• Dawada la xasuusto: Qalabka degdegga ah ee GLUCAGON 1 MG
• Lambarka NDC: 00002803101
• Nambarka (tirada): Dxnumxd
• Taariikhda (yada) uu Dhacayo: April 2022

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacaya 1-800-FDA-0178.

METFORMIN HCL ER 750 MG

Bishii Juun 30, 2021, VIONA PHARMACEUTICALS, INC waxay dib u soo celisay METFORMIN HCL ER 750 MG sababo la xiriira jiritaan aan nadiif ahayn. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray Fasalka II ee daawooyinka ay saameeyeen.
Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: http://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

• Dawada la xasuusto: METFORMIN HCL ER 750 MG
• Lambarka NDC: 72578003601
• Nambarka (tirada): M1915601 iyo M915602
• Taariikhda (yada) uu Dhacayo: Oct 2021

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacaya 1-800-FDA-0178.

BUSPIRONE HCL 15 MG

Bishii Juun 6, 2021, OXFORD PHARMACEUTICALS, LLC waxay dib u soo celisay BUSPIRONE HCL 15 MG sababtoo ah joogitaanka walax shisheeye. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray Fasalka II ee daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: http://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

• Dawada la xasuusto: BUSPIRONE HCL 15 MG
• Lambarka NDC: 69584009310
• Nambarka (tirada): C21021A
• Taariikhda (yada) uu Dhacayo: 03/2023

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacaya 1-800-FDA-0178.

NP THYROID DHAMMAAN XOOGYADA

Bishii Juun 2, 2021, ACELLA PHARMACEUTICALS, LLC waxay dib u soo celisay NP THYROID awood-hoosaad awgood. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray Fasalka XNUMX-aad ee daawooyinka ay saameeyeen.
Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: http://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

• Dawada la xasuusto: NP THYROID DHAMMAAN XOOGYADA
• Lambarka NDC: 42192032701, 42192032707, 42192032901, 42192032907, 42192033001, 42192033101, 42192032801, 42192032807

Sababtoo ah mugga badan ee lambarrada badan ee la saameeyay, fadlan tixraac xiriirka shabakadda FDA ee kor ku xusan si aad u hesho macluumaad gaar ah oo ku saabsan tirada badan ee la xiriirta daawadaada.

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacaya 1-800-FDA-0178.

HALOPERIDOL DECANOATE 50 MG / ML iyo 100 MG / ML

Bishii Meey 26, 2021, TEVA PHARMACEUTICALS waxay dib u soo celisay HALOPERIDOL DECANOATE sababo la xiriira suurtagalnimada jiritaanka wasakh. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray Fasalka II ee daawooyinka ay saameeyeen.
Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: http://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

• Dawada la xasuusto: HALOPERIDOL DECANOATE 50 MG / ML iyo 100 MG / ML
• Lambarka NDC: 00703712103, 00703713103
• Nambarka (tirada): 31325793C, 31325394C, 31327161B
• Taariikhda (s): 09/2021, 04/2022

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacaya 1-800-FDA-0178.

ESTRADIOL (TODDOBAADKII LABAAD) .0375MG / 24 HR PATCH

Abriil 28, 2021, NOVEN PHARMACEUTICAL, INC. Waxay dib uxasuusatay ESTRADIOL (TODOBAADKA LABAAD) .0375MG / 24 HR PATCH iyadoo ay ugu wacan tahay suurtagalnimada in balastarku cilladaysan yahay. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray Fasalka II ee daawooyinka ay saameeyeen.
Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: http://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

• Dawada lagu xasuusto: ESTRADIOL (TODDOBAAD LABAAD) .0375MG / 24 HR PATCH
• Nambarka NDC: 68968343708
• Nambarka (tirada): 88321
• Taariikhda (s): 02 / 2022

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacaya 1-800-FDA-0178.

MAALMAHA DAYTRANA

Bishii Juun 2, 2021, NOVEN PHARMACEUTICAL, INC. Waxay dib u xasuusatay DAYTRANA 10 MG iyo 15 MG PATCHES sababo la xiriira suurtagalnimada in balastarka cilladaysan. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray Fasalka II ee daawooyinka ay saameeyeen.
Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: http://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

• Dawada la xasuusto: DAYTRANA 10 MG iyo 15 MG
• Lambarka NDC: 68968555201, 68968555203, 68968555301, 68968555303
• Nambarka (tirada): 88528, 88530
• Taariikhda (yada) uu Dhacayo: 09 / 2021, 10 / 2021

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacaya 1-800-FDA-0178.

CEFPROZIL 250 MG / 5ML

Bishii Abriil 21, 2021, LUPINE PHARMACEUTICALS, INC waxay dib u soo celisay CEFPROZIL 250 MG / 5ML sababo la xiriira awood darri. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray Fasalka II ee daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: http://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

• Dawada la xasuusto: CEFPROZIL 250 MG / 5ML
• Lambarka NDC: 68180040201, 68180040202, 68180040203
• Nambarka (tirada): F801122, F801123, F801124
• Taariikhda (yada) uu Dhacayo: June 2021

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacaya 1-800-FDA-0178.

GUANFACINE 2 MG ER TABLET

Bishii Abriil 14, 2021, APOTEX waxay dib u soo xasuusatay TABLETSKA GUANFACINE 2 MG ER sababo la xiriira is-tallaabidda ka dhalan karta. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray Fasalka II ee daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: http://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

• Dawada lagu xasuusto: GUANFACINE 2 MG ER TABLET
• Lambarka NDC: 60505-3928-01
• Lambarka (tirada): RX1662, RX1663, RX1664
• Taariikhda (s): 11 / 2022

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacaya 1-800-FDA-0178.

MOMETASONE DHAQAALAHA 0.1%

Bishii Abriil 14, 2021, COSETTE PHARMACEUTICALS, INC waxay dib u soo celisay MOMETASONE FUROATE 0.1% sababo la xiriira xoogsheegasho. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray Fasalka II ee daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: http://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

• Dawada la xasuusto: MOMETASONE DHAQAALAHA 0.1%
• Lambarka NDC: 00713-0701-85, 00713-0701-53
• Nambarka (tirada): 1014611, 1014612, 1014593, 1014594, 1014595
• Taariikhda (yada) uu Dhacayo: 10 / 2022, 12 / 2022

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacaya 1-800-FDA-0178.

RIOMET 500 MG / 5ML

Bishii Abriil 21, 2021, SUN FARMAAJO Warshadaha, INC. Waxay dib u xasuusatay RIOMET 500 MG / 5ML arrimo la xiriira faddarayn darteed. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray Fasalka II ee daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: http://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

• Dawada la xasuusto: RIOMET 500 MG / 5ML
• Lambarka NDC: 10631020602
• Nambarka (tirada): J190386A, X190354A, A200035A, B200064A, H200236A
• Taariikhda (s): 3/2021, 5/2021, 6/2021, 8/2021, 1/2022

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacaya 1-800-FDA-0178.

DAYTRANA PATCH

Maarso 10, 2021, NOVEN PHARMACEUTICALS, INC. Waxay dib u xasuusatay Daytrana sababo la xiriira suurtagalnimada nidaam gaarsiinta cilladaysan. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray Fasalka II ee daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: http://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

• Dawada la xasuusto: DAYTRANA
• Lambarka NDC: 68968555203, 68968555303, 68968555403, 68968555503
• Nambarka (tirada): 87579, 88243, 87818, 88274, 88531
• Taariikhda (yada) uu Dhacayo: 3/2021, 7/2021, 4/2021, 5/2021, 7/2021

Waxa ay tahay inaad sameyso:

• Haddii aad daawada leedahay, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii tirada badan ee aad heshay ay qayb ka tahay xusuusintan iyo tilmaamo dheeraad ah.
• Dhacdooyinka xun ee ka yimaada isticmaalka dawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacaya 1-800-FDA-0178.

FAMOTIDINE 40 MG FADHIYADA

Bishii Maarso 10, 2021, AUROBINDO PHARMA waxay dib u soo celisay FAMOTIDINE 40MG sababo la xiriira suurta galnimada isku-darka kiniinka. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray Fasalka II ee daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: http://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

• Dawada la xasuusto: FAMOTIDINE 40 MG
• Lambarka NDC: 65862-0860-99
• Nambarka (yada) badan: P2000467
• Taariikhda (yada) uu Dhacayo: 7/2022

Waxa ay tahay inaad sameyso:

• Haddii aad daawada leedahay, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii tirada badan ee aad heshay ay qayb ka tahay xusuusintan iyo tilmaamo dheeraad ah.
• Dhacdooyinka xun ee ka yimaada isticmaalka dawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacaya 1-800-FDA-0178.

IMATINIB MESYLATE 100 MG

Markay ahayd Marso 2, 2021 DR. REDDY's LAB waxay dib uxasuusatay IMATINIB MESYLATE 100 MG sababo laxiriira kala dirista oo kufashilmay. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray Fasalka II ee daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: http://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

• Dawada la xasuusto: IMATINIB MESYLATE 100 MG
• Lambarka NDC: 43598034490, 43598034431
• Nambarka (tirada): H2000206, H2000138
• Taariikhda (yada) uu Dhacayo: 06/2022

Waxa ay tahay inaad sameyso:

• Haddii aad daawada leedahay, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii tirada badan ee aad heshay ay qayb ka tahay xusuusintan iyo tilmaamo dheeraad ah.
• Dhacdooyinka xun ee ka yimaada isticmaalka dawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacaya 1-800-FDA-0178.

OMEPRAZOLE 20 MG

Bishii Maarso 24, 2021, BRECKENRIDGE waxay dib u soo celisay OMEPRAZOLE 20 MG sababo la xiriira jiritaanka wax aan nadiif ahayn. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray Fasalka II ee daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: http://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

• Dawada la xasuusto: OMEPRAZOLE 20 MG
• Lambarka NDC: 51991064310
• Nambarka (tirada): 191659
• Taariikhda (yada) uu Dhacayo: 05/20/21

Waxa ay tahay inaad sameyso:

• Haddii aad qaadatay daawada, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii lambarka tirada badan ee aad heshay uu qayb ka yahay xusuusintan iyo tilmaamo dheeraad ah
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacaya 1-800-FDA-0178

Cirbadaha Sodium Enoxaparin 100mg / mL iyo Enoxaparin Sodium Cirbada 120mg / 0.8mL

Bishii Febraayo 18, 2021, Shirkadda Apotex waxay dib u soo celisay Enoxaparin Sodium sababo la xiriira isku-darka calaamadeynta ah. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray Fasalka XNUMX-aad ee daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: http://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

• Dawada la xasuusto: Cirbadaha Sodium Enoxaparin 100mg / mL iyo Enoxaparin Sodium Cirbada 120mg / 0.8mL
• Lambarka NDC: 60505079604, 60505079600, 60505079504, 60505079501
• Nambarka (tirada): CS008, CT003
• Taariikhda (yada) uu Dhacayo: 04 / 2022, 05 / 2022

Waxa ay tahay inaad sameyso:

• Haddii aad daawada leedahay, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii tirada badan ee aad heshay ay qayb ka tahay xusuusintan iyo tilmaamo dheeraad ah.
• Dhacdooyinka xun ee ka yimaada isticmaalka dawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacaya 1-800-FDA-0178.

Metformin ER 750 mg

Bishii Febraayo 10, 2021, Nostrum Laboratories, Inc. ayaa dib u soo celisay Metformin ER 750mg sababo la xiriira jiritaanka wasakh. Maamulka Cuntada iyo Dawooyinka ee Maraykanka (FDA) ayaa soo saaray a Soocelinta Heerka II daawooyinka ay saameysay.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: http://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

• Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:
  Dawada la xasuusto: METFORMIN HCL ER 750 MG
• Lambarka NDC: 29033005601
• Nambarka (tirada): MET200601
• Taariikhda (yada) uu Dhacayo: 07/2022

Waxa ay tahay inaad sameyso:

• Haddii aad daawada leedahay, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii tirada badan ee aad heshay ay qayb ka tahay xusuusintan iyo tilmaamo dheeraad ah.
• Dhacdooyinka xun ee ka imanaya isticmaalka dawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA iyaga oo booqanaya www.fda.gov/medwatch/report.htm ama soo waca 1-800-FDA-0178.

Nortriptyline 10mg Kaabsal

Bishii Febraayo 10, 2021, Taro Pharmaceuticals USA, Inc. waxay dib u soo celisay kaabsoolayaasha 10mg ee Nortriptyline sababtoo ah jiritaanka wasakh. Maamulka Cunnada iyo Dawooyinka ee Maraykanka (FDA) ayaa soo saaray Fasalka II ee dawooyinka ay dhibaatadu soo gaadhay.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: http://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

• Dawada la xasuusto: NORTRIPTYLINE HCL 10 MG
• Lambarka NDC: 51672-4001-01
• Nambarka (tirada): AC05096, AC05098, iyo AC05099
• Taariikhda (yada) uu Dhacayo: 10/31/2022

Waxa ay tahay inaad sameyso:

• Haddii aad daawada leedahay, fadlan la xiriir farmasiga aad ka heshay si aad u hubiso haddii tirada badan ee aad heshay ay qayb ka tahay xusuusintan iyo tilmaamo dheeraad ah.

• Dhacdooyinka xun ee ka yimaada isticmaalka dawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacaya 1-800-FDA-0178.

PAROEX 0.12%

Bishii Diseembar 2, 2020, SUNSTAR AMERICA waxay dib u soo celisay PAROEX 0.12% sababo la xiriira iskudhafan kiniin ah. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray Fasalka Koowaad ee daawooyinka ay saameeyeen.
Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: http://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:
Dawada la xasuusto: PAROEX 0.12%
Lambarka NDC: 52376002102
Sababtoo ah mugga badan ee lambarrada badan ee la saameeyay, fadlan tixraac bogga shabakadda FDA ee kor ku xusan si aad u hesho macluumaad gaar ah oo ku saabsan tirada badan ee la xiriirta daawadaada.

Waxa ay tahay inaad sameyso:

• Ha u sii wadin isticmaalka PAROEX 0.12% haddii dib loogu yeeray
• Hubi calaamadda daawadaada si aad u aragto haddii aad leedahay wax PAROEX ah oo ku jira lambarrada saamaynta ku leh iyo taariikhaha ay dhacayaan.
• Haddii aad daawada leedahay, la xiriir farmasiga aad ka heshay. Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacaya 1-800-FDA-0178.

MESALAMINE 1.2 G

Markay ahayd 11/18/2020, ACTAVIS / TEVA waxay dib uxasuusatay MESALAMINE iyadoo ay ugu wacan tahay jiritaanka wasakhda. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray soocelin heer labaad ah oo ku saabsan dawooyinka ay saameeyeen.
Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: http://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: MESALAMINE 1.2 G
Lambarka NDC: 00591-2245-22
Sababtoo ah mugga badan ee lambarrada Luud ee ay saameeyeen, fadlan tixraac bogga shabakadda FDA ee kor ku xusan si aad u hesho macluumaad gaar ah oo ku saabsan tirada badan ee la xiriirta daawadaada.

Waxa ay tahay inaad sameyso:

• Ha u sii wadin isticmaalka MESALAMINE 1.2 G haddii dib loo xusuusto.
• Hubi calaamadda daawada laguu qoray si aad u aragto haddii aad hayso MESALAMINE lambarrada saamaynta badan ee ay saamaysay iyo
taariikhaha uu dhacayo
• Haddii aad daawada leedahay, la xiriir farmasiga aad ka heshay.
• Dhacdooyinka xun ee ka yimaada isticmaalka dawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacaya 1-800-FDA-0178.

NP THYROID 15mg iyo 120mg

Bishii Oktoobar 28, 2020, ACELLA PHARMACEUTICALS, LLC waxay dib u soo celisay NP THYROID 15mg iyo 120mg sababo la xiriira awood-hoosaadyo. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray Fasalka XNUMX-aad ee daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: http://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto:               NP THYROID 15mg iyo 120mg
Lambarka NDC:                42192-0327-01, 42192-0328-01
Nambarka (tirada):              M327E19-1, M328F19-3
Taariikhda (yada) uu Dhacayo:      10 / 2020, 11 / 2020

Waxa ay tahay inaad sameyso:

• Ha u sii wadin isticmaalka NP Thyroid haddii dib loo xusuusto
• Hubi calaamadda daawada laguu qoray si aad u aragto haddii aad leedahay wax LISINOPRIL ah oo ku jira lambarrada saamaynta ku leh iyo taariikhaha ay dhacayaan.
• Haddii aad qaadatay daawada, la xiriir farmasiga aad ka heshay. Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya www.fda.gov/medwatch/report.htm ama wacaya 1-800-FDA-0178.

QAADASHADA 5 MCG / HR

Oktoobar 7, 2020, TEVA USA waxay dib uxasuusatay BUPRENORPHINE sababo laxiriira awood hoose. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray soocelin heer labaad ah oo ku saabsan dawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: http://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto:               QAADASHADA 5 MCG / HR
Lambarka NDC:                00093365640
Nambarka (tirada):              190017, 190161
Taariikhda (yada) uu Dhacayo:         02 / 2021, 08 / 2021

Waxa ay tahay inaad sameyso:

• Ha u sii wadin isticmaalka BUPRENORPHINE 5 MCG / HR haddii dib loo soo xusuusiyay.
• Hubi calaamadda daawada laguu qoray si aad u aragto haddii aad leedahay BUPRENORPHINE-ka lambarrada badan ee waxyeellada soo gaadhay iyo taariikhda uu dhacayo.
• Haddii aad qaadatay daawada, la xiriir farmasiga aad ka heshay.
• Dhacdooyinka xun ee ka imanaya isticmaalka dawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya fda.gov/medwatch/report.htm ama soo waca 1-800-FDA-0178.

MIBELAS 24 FE 1MG-20 (24)

Bishii Ogosto 19, 2020, LUPINE PHARMACEUTICALS waxay dib u soo celisay MIBELAS 24 FE sababo la xiriira jiritaanka wax aan nadiif ahayn. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray CLASS II dib ugu soo celinta daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: http://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto:   MIBELAS 24 FE 1MG-20 (24)
Lambarka NDC:   68180091113
Lambarada Lot:    L900017, L900070, L900589, L901085, L901008, L901641, L901735
Taariikhda uu dhacayo:  12/31/2020, 3/31/2021, 4/30/2021, 6/30/2021, 10/31/2021

Waxa ay tahay inaad sameyso:

• Ha u sii wadin isticmaalka MIBELAS 24 FE 1MG-20 (24) haddii dib loo soo xusuusiyay.
• Hubi calaamadda daawadaada si aad u aragto haddii aad mid ka mid ah MIBELAS 24 FE oo ku jirta lambarrada saamaynta ku leh iyo taariikhda uu dhacayo.
• Haddii aad qaadatay daawada, la xiriir farmasiga aad ka heshay.
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya fda.gov/medwatch/report.htm ama wacaya 1-800-FDA-0178.

Metformin ER 500mg iyo 1000mg kiniinno
(Waxaa soo saaray Lupine Pharmaceuticals)

Bishii Luulyo 22, 2020, Daawooyinka Lupine waxay dib u soo celiyeen Metformin ER 750mg iyo 1000mg sababtoo ah jiritaanka wasakh. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray Fasalka II ee daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: http://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: Metformin ER 500mg iyo 1000mg
Lambarka NDC: 68180033801, 68180033607, 68180033909, 68180033707
Maaddaama tirada badan ee lambarrada Luuddu ay saamaysay, fadlan tixraac bogga shabakadda ee FDA ee kor ku xusan si aad u hesho macluumaad gaar ah oo ku saabsan tirada (tirada) iyo taariikhda uu dhacayo ee la xiriirta daawadaada.

Waxa ay tahay inaad sameyso:

• Ha u sii wadin isticmaalka Metformin ER 750mg ama 1000mg haddii dib loo xusuusto.
• Hubi calaamadda daawada laguu qoray si aad u aragto haddii aad leedahay mid ka mid ah lambarrada saamaynta badan ee dhacay iyo taariikhda uu dhacayo.
• Haddii aad qaadatay daawada, la xiriir farmasiga aad ka heshay. Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya fda.gov/medwatch/report.htm ama wacaya 1-800-FDA-0178.

Metformin ER 750 mg
(waxaa soo saaray Granules Pharmaceuticals)

7/22/2020, Daawooyinka Granules dib ayuu u xasuustay Metformin ER sababo la xiriira jiritaanka wasakh. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray soocelin heer labaad ah oo ku saabsan dawooyinka ay saameeyeen

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: http://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto:   Metformin ER
Lambarka NDC:     70010-0492-01, 70010-0492-05
Maaddaama tirada badan ee lambarrada Luuddu ay saamaysay, fadlan tixraac bogga shabakadda ee FDA ee kor ku xusan si aad u hesho macluumaad gaar ah oo ku saabsan tirada (tirada) iyo taariikhda uu dhacayo ee la xiriirta daawadaada.

Waxa ay tahay inaad sameyso:

• Ha u sii wadin isticmaalka Metformin ER 750mg haddii dib loo xusuusto.
• Hubi calaamadda daawada laguu qoray si aad u aragto haddii aad wax Metformin ER ah ku leedahay lambarrada saamaynta ku leh iyo taariikhaha ay dhacayaan.
• Haddii aad qaadatay daawada, la xiriir farmasiga aad ka heshay.
• Dhacdooyinka xun ee ka imanaya isticmaalka dawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya fda.gov/medwatch/report.htm ama soo waca 1-800-FDA-0178.

AURYXIA 210MG MIISAANKA

Bishii Luulyo 22, 2020 KERYX BIOPHARMACEUTICALS ayaa dib u soo celisay AURYXIA sababo la xiriira hubin la'aan tayo sida ay go'aamisay FDA. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray soocelin heer labaad ah oo ku saabsan dawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: http://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto:   AURYXIA 210MG IRON
Lambarka NDC:     59922063101
Maaddaama tirada badan ee lambarrada Luuddu ay saamaysay, fadlan tixraac bogga shabakadda ee FDA ee kor ku xusan si aad u hesho macluumaad gaar ah oo ku saabsan tirada (tirada) iyo taariikhda uu dhacayo ee la xiriirta daawadaada.

Waxa ay tahay inaad sameyso:

• Ha u sii wadin isticmaalka AURYXIA 210MG IRON haddii dib loo soo xusuusiyay.
• Hubi calaamadda daawadaada si aad u aragto haddii aad qabtid wax AURYXIA ah oo ku jira lambarrada saamaynta ku leh iyo taariikhaha ay dhacayaan.
• Haddii aad qaadatay daawada, la xiriir farmasiga aad ka heshay.
• Dhacdooyinka xun ee ka imanaya isticmaalka dawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya fda.gov/medwatch/report.htm ama soo waca 1-800-FDA-0178.

LISINOPRIL 10 MG

Bishii Ogosto 5, 2020, SHAQAALOOYINKA BLUEPOINT waxay dib u soo celiyeen LISINOPRIL 10 MG sababo la xiriira isku-darka kiniinka. Maamulka Cunnada iyo Dawooyinka ee Maraykanka (FDA) ayaa soo saaray Fasalka II ee dawooyinka ay dhibaatadu soo gaadhay.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: http://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto:LISINOPRIL 10 MG
Lambarka NDC:68001033408
Lambarada Lot:  Q000232
Taariikhda uu dhacayo:  01/2022

Waxa ay tahay inaad sameyso:

• Ha u sii wadin isticmaalka LISINOPRIL 10 MG haddii dib loo soo xusuusiyay
• Hubi calaamadda daawada laguu qoray si aad u aragto haddii aad leedahay wax LISINOPRIL ah oo ku jira lambarrada saamaynta ku leh iyo taariikhaha ay dhacayaan.
• Haddii aad qaadatay daawada, la xiriir farmasiga aad ka heshay. Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya fda.gov/medwatch/report.htm ama wacaya 1-800-FDA-0178.

Metformin ER 500mg iyo 750mg

soosaarayaal badan ayaa dib loo soo celinayaa Metformin 500mg iyo 700mg Kiniinno Lagu Sii Daayay joogitaanka wasakhda darteed. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray soocelin heer labaad ah oo ku saabsan dawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: http://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: Metformin ER 500mg iyo 750mg
Lambarka NDC: Maaddaama ay aad u sarreeyaan tirooyinka NDC ee ay saameysey, fadlan tixraac xiriiriye websaydhka FDA ee kor ku xusan si aad u hesho macluumaad gaar ah oo ku saabsan NDC (yada), lambarro aad u tiro badan iyo taariikhda uu dhacayo ee la xiriirta daawadaada.

Waxa ay tahay inaad sameyso:

• Ha usii wadin inaad isticmaasho wax daawo ah oo dib loo xasuusto.
• Hubi calaamadda daawada laguu qoray si aad u aragto haddii aad leedahay Metformin ER 500mg ama 750mg oo ku jira lambarrada saamaynta ku leh iyo taariikhaha ay dhacayaan.
• Haddii aad qaadatay daawada, la xiriir farmasiga aad ka heshay.
• Dhacdooyinka xun ee ka imanaya isticmaalka dawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya fda.gov/medwatch/report.htm ama soo waca 1-800-FDA-0178.

NP Thyroid 30mg, 60mg, 90mg

Bishii Juun 10, 2020, Acella Pharmaceuticals, LLC, waxay dib u soo celisay NP Thyroid sababtoo ah awood-hoosaad. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray Fasal aan dib ugu xasuusto dawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: http://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto:               NP Thyroid 30mg, 60mg, 90mg
Lambarada NDC:              42192032901, 42192033001, 42192033101
Lambarada Lot:                M329H18-1, M329J18-1, M329J18-2, M329J18-3, M329M18-2, M329A19-1, M330J18-2A, M330J18-3, M331G18-1, M331J18-1, M331J18-2, M331M18-1, M331M18-2
Taariikhaha Dhamaadka:          Juun-2020, JUL-2020, AUG-2020, NOV-2020, DEC-2020

Waxa ay tahay inaad sameyso:

• Ha u sii wadin isticmaalka NP Thyroid haddii dib loo xusuusto.
• Hubi calaamadda daawada laguu qoray si aad u aragto haddii aad leedahay mid ka mid ah lambarrada saamaynta badan ee dhacay iyo taariikhda uu dhacayo.
• Haddii aad qaadatay daawada, la xiriir farmasiga aad ka heshay.
• Dhacdooyinka xun ee ka imanaya isticmaalka dawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya fda.gov/medwatch/report.htm ama soo waca 1-800-FDA-0178.

Kiniiniyada Mirtazapine 15mg

Bishii Abriil 22, 2020, Aurobindo Pharma USA, Inc., waxay dib u soo celisay kiniiniyada MIRTAZAPINE 15mg sababo la xiriira suurtagalnimada faddarayn. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray soocelin heer labaad ah oo ku saabsan dawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: http://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto:               Mirtazapine 15 mg
Lambarka NDC:                13107-0031-34, 65862-0198-99
Lambarada Lot:                 031180028A
Taariikhda uu dhacayo:            03/2021

Waxa ay tahay inaad sameyso:

• Ha u sii wadin isticmaalka MIRTAZAPINE 15mg haddii dib loo soo xusuusiyay.
• Hubi calaamadda daawada laguu qoray si aad u aragto haddii aad leedahay mid ka mid ah lambarrada saamaynta badan ee dhacay iyo taariikhda uu dhacayo.
• Haddii aad qaadatay daawada, la xiriir farmasiga aad ka heshay. Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya fda.gov/medwatch/report.htm ama wacaya 1-800-FDA-0178.

Oxycodone / acetaminophen kiniiniyada 10 / 325mg

Bishii Abriil 22, 2020, Aurobindo Pharma USA, Inc., waxay dib u soo celisay kiniinnada OXYCODONE / ACETAMINOPHEN 10 / 325mg sababo la xiriira suurtagalnimada faddarayn. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray soocelin heer labaad ah oo ku saabsan dawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: http://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto:               Oxycodone / acetaminophen 10 / 325mg
Lambarka NDC:                13107-0046-01
Lambarada Lot:                 046180056A
Taariikhda uu dhacayo:            05/2020

Waxa ay tahay inaad sameyso:

• Ha usii wadin isticmaalka OXYCODONE / ACETAMINOPHEN haddii dib loogu yeeray.
• Hubi calaamadda daawada laguu qoray si aad u aragto haddii aad leedahay mid ka mid ah lambarrada saamaynta badan ee dhacay iyo taariikhda uu dhacayo.
• Haddii aad qaadatay daawada, la xiriir farmasiga aad ka heshay. Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya fda.gov/medwatch/report.htm ama wacaya 1-800-FDA-0178.

Kiniiniyada Mirtazapine 15mg

Bishii Abriil 22, 2020, Aurobindo Pharma USA, Inc., waxay dib u soo celisay kiniiniyada MIRTAZAPINE 15mg sababo la xiriira suurtagalnimada faddarayn. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray soocelin heer labaad ah oo ku saabsan dawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: http://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto:               Mirtazapine 15 mg
Lambarka NDC:                13107-0031-34, 65862-0198-99
Lambarada Lot:                 031180028A
Taariikhda uu dhacayo:            03/2021

Waxa ay tahay inaad sameyso:

• Ha u sii wadin isticmaalka MIRTAZAPINE 15mg haddii dib loo soo xusuusiyay.
• Hubi calaamadda daawada laguu qoray si aad u aragto haddii aad leedahay mid ka mid ah lambarrada saamaynta badan ee dhacay iyo taariikhda uu dhacayo.
• Haddii aad qaadatay daawada, la xiriir farmasiga aad ka heshay. Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya fda.gov/medwatch/report.htm ama wacaya 1-800-FDA-0178.

LISINOPRIL 30 MG

Bishii Abriil 8, 2020, LUPINE PHARMACEUTICALS, INC. Waxay dib u xasuusatay LISINOPRIL sababo la xiriira suurtagalnimada isku-darka kiniinka. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray soocelin heer labaad ah oo ku saabsan dawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: http://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto:               LISINOPRIL 30 MG
Lambarka NDC:                68180098201
Lambarada Lot:                Q900580
Taariikhda uu dhacayo:            9/2021

Waxa ay tahay inaad sameyso:

• Ha u sii wadin isticmaalka LISINOPRIL 30 MG haddii dib loo soo xusuusiyay.
• Hubi calaamadda daawada laguu qoray si aad u aragto haddii aad mid ka mid ah lambarrada saamaynta ku leh iyo taariikhaha ay dhacayaan.
• Haddii aad qaadatay daawada, la xiriir farmasiga aad ka heshay.
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya fda.gov/medwatch/report.htm ama wacaya 1-800-FDA-0178.

Kiniiniyada Levetiracetam 750mg

Bishii Abriil 22, 2020, Aurobindo Pharma USA, Inc., waxay dib u soo celisay LEVETIRACETAM 750mg sababo la xiriira suurtagalnimada faddarayn. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray soocelin heer labaad ah oo ku saabsan dawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: http://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto:     Levetiracetam 750mg
Lambarka NDC:    65862-0053-90
Lambarada Lot:      24719001A1
Taariikhda uu dhacayo:   03/2021

Waxa ay tahay inaad sameyso:

• Ha u sii wadin isticmaalka LEVETIRACETAM 750mg haddii dib loo xusuusto
• Hubi calaamadda daawada laguu qoray si aad u aragto haddii aad leedahay mid ka mid ah lambarrada saamaynta badan ee dhacay iyo taariikhda uu dhacayo.
• Haddii aad qaadatay daawada, la xiriir farmasiga aad ka heshay. Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya fda.gov/medwatch/report.htm ama wacaya 1-800-FDA-0178.

GLYCOPYRRATE 1 MG

Abriil 8, 2020, FAR FARMAAJO. dib loogu xasuusto GLYCOPYRRATE 1 MG sababo la xiriira jiritaanka wasakh. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray soocelin heer labaad ah oo ku saabsan dawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: http://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto:  GLYCOPYRRATE 1 MG
Lambarka NDC:   49884006501
Lambarada Lot:    32809101
Taariikhda uu dhacayo:  3/2021

Waxa ay tahay inaad sameyso:

• Ha u sii wadin isticmaalka GLYCOPYRRATE 1 MG haddii dib loo soo xusuusiyay
• Hubi calaamadda daawada laguu qoray si aad u aragto haddii aad mid ka mid ah lambarrada saamaynta ku leh iyo taariikhaha ay dhacayaan.
• Haddii aad qaadatay daawada, la xiriir farmasiga aad ka heshay. Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya fda.gov/medwatch/report.htm ama wacaya 1-800-FDA-0178.

Gabapentin 100mg Kaabsal

Bishii Abriil 22, 2020, Aurobindo Pharma USA, Inc., waxay dib u soo celisay GABAPENTIN 100mg sababo la xiriira suurtagalnimada faddarayn. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray soocelin heer labaad ah oo ku saabsan dawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: http://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto:               Gabapentin 100 mg
Lambarka NDC:                65862-0198-99
Lambarada Lot:                 198180048A, 198180061A, 19819017A1
Taariikhda uu dhacayo:            04/2021, 06/2020, 02/2021

Waxa ay tahay inaad sameyso:

• Ha u sii wadin isticmaalka GABAPENTIN 100mg haddii dib loo xusuusto
• Hubi calaamadda daawada laguu qoray si aad u aragto haddii aad leedahay mid ka mid ah lambarrada saamaynta badan ee dhacay iyo taariikhda uu dhacayo.
• Haddii aad qaadatay daawada, la xiriir farmasiga aad ka heshay. Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya fda.gov/medwatch/report.htm ama wacaya 1-800-FDA-0178.

Daytrana (methylphenidate) 10mg, 20mg, iyo 30mg balastar

Bishii Abriil 29, 2020, Noven Therapeutics, LLC, waxay dib u xasuusatay Daytrana 10mg, 20mg, iyo 30mg sababo la xiriira suurtagalnimada in balastarku cilladaysan yahay. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray soocelin heer labaad ah oo ku saabsan dawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: http://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto:  Daytrana 10mg, 20mg, iyo 30mg
Lambarka NDC: 68968-5552-03, 68968-5554-03, 68968-5555-03
Lambarada Lot:  886647, 86354, 86355, 86356, 86550, 87348, 87965
Taariikhda uu dhacayo: 09/2020, 08/2020, 07/2020, 08/2020, 07/2020, 01/2021. 01/2021

Waxa ay tahay inaad sameyso:

• Ha u sii wadin isticmaalka DAYTRANA 10mg, 20mg, iyo 30mg haddii dib loo xusuusto.
• Hubi calaamadda daawada laguu qoray si aad u aragto haddii aad leedahay mid ka mid ah lambarrada saamaynta badan ee dhacay iyo taariikhda uu dhacayo.
• Haddii aad qaadatay daawada, la xiriir farmasiga aad ka heshay. Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya fda.gov/medwatch/report.htm ama wacaya 1-800-FDA-0178.

Acetaminophen leh Codeine 300 / 15mg, 300 / 30mg, 300 / 60mg

Bishii Abriil 8, 2020, Aurobindo Pharma, USA, Inc., waxay dib u soo celisay acetaminophen oo leh koodhin sababtoo ah faddarayn suurtagal ah. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray soocelin heer labaad ah oo ku saabsan dawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: http://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto:               Acetaminophen leh Codeine 300 / 15mg, 300 / 30mg, 300 / 60mg
Lambarka NDC:                13107005801, 13107005999, 13107006001, 52959000310, 52959000312, 52959000314, 52959000316, 52959000320, 52959000330, 52959000360
Lambarada Lot:                058180015A, 058180016A, 05818017B1, 059180023A, 059180024A, 059180025A, 060180017A, 060180019B1, 060180020A iyo 060180021A
Taariikhda uu dhacayo:            07/2021, 09/2021, 05/2021, 06/2021

Waxa ay tahay inaad sameyso:

• Ha u sii wadin isticmaalka mid ka mid ah daroogada ay saameysay haddii dib loo xusuusto.
• Hubi calaamadda daawada laguu qoray si aad u aragto haddii aad leedahay mid ka mid ah lambarrada saamaynta badan ee dhacay iyo taariikhda uu dhacayo.
• Haddii aad qaadatay daawada, la xiriir farmasiga aad ka heshay.
• Dhacdooyinka xun ee ka imanaya isticmaalka dawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya fda.gov/medwatch/report.htm ama soo waca 1-800-FDA-0178.

Daytrana (methylphenidate) 10mg, 15mg, 20mg, iyo 30mg balastar

Bishii Maarso 25, 2020, Noven Therapeutics Associates, Inc., waxay dib u xusuusisay Daytrana iyadoo ay ugu wacan tahay suurtagalnimada in balastarka uu cilladaysan yahay. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray soocelin heer labaad ah oo ku saabsan dawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: http://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto:            Daytrana Patches (dhammaan awooda)
Lambarka (yada) NDC:        68968555203, 68968555303, 68968555403, 68968555503
Nambarka (tirada):           86280, 85942, 86281, 86081, 86196, 86083, 86282
Taariikhda uu dhacayo:         06/2020, 03/2020, 06/2020, 04/2020, 05/2020, 06/2020

Waxa ay tahay inaad sameyso:

• Ha u sii wadin isticmaalka daawada haddii dib loo xusuusto.
• Hubi calaamadda daawada laguu qoray si aad u aragto haddii aad leedahay mid ka mid ah lambarrada saamaynta badan ee dhacay iyo taariikhda uu dhacayo.
• Haddii aad qaadatay daawada, la xiriir farmasiga aad ka heshay.
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya fda.gov/medwatch/report.htm ama wacaya 1-800-FDA-0178.

Sotalol AF 80mg

Bishii Maarso 25, 2020, Daawooyinka Mylan waxay dib uxasuusteen Sotalol sababo la xiriira joogitaanka wasakhda. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray soocelin heer labaad ah oo ku saabsan dawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: http://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto:         Sotalol AF 80mg
Lambarka NDC:            00378512301
Lambarka Naadiga:              3095754
Taariikhda uu dhacayo:     02/2021

Waxa ay tahay inaad sameyso:

• Ha u sii wadin isticmaalka daawada haddii dib loo xusuusto.
• Hubi calaamadda daawada laguu qoray si aad u aragto haddii aad leedahay mid ka mid ah lambarrada saamaynta badan ee dhacay iyo taariikhda uu dhacayo.
• Haddii aad qaadatay daawada, la xiriir farmasiga aad ka heshay.
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya fda.gov/medwatch/report.htm ama wacaya 1-800-FDA-0178.

Phenytoin 125mg / 5mL ganaax afka ah

Bishii Febraayo 21, 2020, Taro Pharmaceuticals, USA, Inc., waxay dib u soo celisay Phenytoin 125mg / 5mL sababo la xiriira awood xagga awoodda ah. Tani waa soo-celin iskaa wax u qabso ah oo ka timid soo-saaraha, sidaa darteed, waxaa loola dhaqmayaa sidii Xusuustii Class I.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: Website-ka FDA.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto:                Phenytoin 15mg / 5mL
Lambarka NDC:                 51672-4069-01
Lambarada Lot:                   327874, 327876
Taariikhda uu dhacayo:             December 2020

Waxa ay tahay inaad sameyso:

• Ha u sii wadin isticmaalka daawada haddii dib loo xusuusto.
• Hubi calaamadda daawada laguu qoray si aad u aragto haddii aad leedahay qaar ka mid ah lambarrada saamaynta badan ee ay saamaysay iyo taariikhda uu dhacayo.
• Haddii aad qaadatay daawada, la xiriir farmasiga aad ka heshay. Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya fda.gov/medwatch/report.htm ama wacaya 1-800-FDA-0178.

Ranitidine 150mg iyo 300mg Kiniinno

Markay ahayd Janaayo 15, 2020, shirkadda dawooyinka ee Glenmark waxay dib u soo celisay kiniiniyada Ranitidine sababo la xiriira joogitaanka nijaasta. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray soocelin heer labaad ah oo ku saabsan dawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: Website-ka FDA.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto:                Ranitidine 150mg iyo 300mg Kiniinno
Lambarka (yada) NDC:            68462024860, 68462024801, 68462024930, 68462024901, 68462024920, 68462024805, 70518171400, 65162025310
Sababtoo ah tirada badan ee lambarrada badan ee la saameeyay, fadlan tixraac xiriirka shabakadda FDA ee kor ku xusan si aad u hesho macluumaad gaar ah oo ku saabsan tirada badan ee la xiriirta daawadaada.

Waxa ay tahay inaad sameyso:

• Ha u sii wadin isticmaalka daawada haddii dib loo xusuusto.
• Hubi calaamadda daawada laguu qoray si aad u aragto haddii aad leedahay mid ka mid ah lambarrada saamaynta badan ee dhacay iyo taariikhda uu dhacayo.
• Haddii aad qaadatay daawada, la xiriir farmasiga aad ka heshay.
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya fda.gov/medwatch/report.htm ama wacaya 1-800-FDA-0178.

Lamotrigine 100mg Kiniin

Bishii Janaayo 10, 2020, Taro Pharmaceuticals USA, Inc., waxay dib u soo celisay LAMOTRIGINE 100MG sababtoo ah faddarayn is-dhaafsi ah. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) weli ma aysan soo saarin dib u soo celinta daawooyinka ay dhibaatadu saameysey, hase yeeshe, shirkaddu waxay si iskood ah u soo xasuusatay tirada badan ee hoos ku dhacday ee heerka macaamiisha.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.fda.gov/drugs/drugsafety/drugRecalls/default.htm

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto:                Lamotrigine 100 mg
Lambarka NDC:                 51672-4131-01
Nambarka (tirada):               331771
Taariikhda uu dhacayo:             Juun, 2021

Waxa ay tahay inaad sameyso:

• Ha u sii wadin isticmaalka daawada Lamotrigine 100mg haddii dib loo soo xusuusiyay.
• Hubi calaamadda daawada laguu qoray si aad u aragto haddii aad leedahay mid ka mid ah lambarrada saamaynta badan ee dhacay iyo taariikhda uu dhacayo.
• Haddii aad qaadatay daawada, la xiriir farmasiga aad ka heshay.
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya fda.gov/medwatch/report.htm ama wacaya 1-800-FDA-0178.

Blisovi FE 1.5 / 30mg, 21 Kiniin ah xirmo kasta

Bishii Janaayo 15, 2020, Lupine Pharmaceuticals waxay dib u xasuusisay Blisovi FE sababo la xiriira cabashooyinka la xiriira burburka kiniinnada markii ay ka soo baxeen xirmada finka. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray soocelin heer labaad ah oo ku saabsan dawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: http://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto:                BLISOVI FE 1.5-30 (21)
Lambarka NDC:                 68180086611
Nambarka (tirada):               H801227
Taariikhda uu dhacayo:             January, 2020

Waxa ay tahay inaad sameyso:

• Ha u sii wadin isticmaalka daawadan haddii dib loo xusuusto.
• Hubi calaamadda daawada laguu qoray si aad u aragto haddii aad leedahay mid ka mid ah lambarrada saamaynta badan ee dhacay iyo taariikhda uu dhacayo.
• Haddii aad qaadatay daawada, la xiriir farmasiga aad ka heshay.
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya fda.gov/medwatch/report.htm ama wacaya 1-800-FDA-0178.

Nystatin Afka Laga Joojiyo 10,000 oo unug mL

Bishii Febraayo 5, 2020, Daawada Associates, Inc., waxay dib u soo celisay Nystatin Oral Suspension 10,000 unug halkii mL sababo la xiriira arrimo awood-hoosaad. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray soocelin heer labaad ah oo ku saabsan dawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: http://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto:                NYSTATIN 100000 / ML
Lambarka NDC:                 00121081016
Lambarada Lot:                   BB70, BB71
Taariikhda uu dhacayo:             2020 karaa

Waxa ay tahay inaad sameyso:

• Ha u sii wadin isticmaalka daawadan haddii dib loo xusuusto
• Hubi calaamadda daawada laguu qoray si aad u aragto haddii aad leedahay mid ka mid ah lambarrada saamaynta badan ee dhacay iyo taariikhda uu dhacayo.
• Haddii aad qaadatay daawada, la xiriir farmasiga aad ka heshay. Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya fda.gov/medwatch/report.htm ama wacaya 1-800-FDA-0178.

Bishii Diseembar 9, 2019, Amneal Pharmaceuticals, Inc., waxay dib u soo celisay kaniiniyada Ranitidine 150mg iyo 350mg, iyo sidoo kale Ranitidine 15mg / mL xal afka ah, sababtoo ah jiritaanka wasakh. Maamulka Cuntada iyo Dawooyinka ee Maraykanka (FDA) ayaa soo saaray a Fasalka II Dib u xasuusashada dawooyinka ay dhibaatadu saameysey.

Macluumaad dheeraad ah oo ku saabsan dib u celinta waxaa laga heli karaa Website-ka FDA. 

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto:                 Ranitidine 150mg, kiniiniyada 300mg, 15mg / mL xal afka ah
Lambarka NDC:                  65162-253-06, 65162-253-10, 65162-253-18, 65162-253-50, 65162-253-11, 65162-254-30, 65162-254-10, 65162-254-25, 65162-664-90
Sababtoo ah mugga badan ee lambarrada Luud ee ay saameeyeen, fadlan tixraac bogga shabakadda FDA ee kor ku xusan si aad u hesho macluumaad gaar ah oo ku saabsan tirada badan ee la xiriirta daawadaada.

Waxa ay tahay inaad sameyso:

• Ha u sii wadin isticmaalka daawada haddii dib loo xusuusto.
• Hubi calaamadda daawada laguu qoray si aad u aragto haddii aad leedahay mid ka mid ah lambarrada saamaynta badan ee dhacay iyo taariikhda uu dhacayo.
• Haddii aad qaadatay daawada, la xiriir farmasiga aad ka heshay.
• Dhacdooyinka xun ee isticmaalka daawooyinka dhakhtarku qoro waa in lagu soo wargeliyaa FDA adoo booqanaya fda.gov/medwatch/report.htm ama wacaya 1-800-FDA-0178.

Bishii Diseembar 27, 2019, Shirkadda Lanett, Inc. waxay dib u soo celisay Levetiracetam 100mg / mL faddarayn darteed. Maamulka Cuntada iyo Dawooyinka ee Maraykanka (FDA) ayaa soo saaray a Fasalka I Dib u xasuusashada dawooyinka ay dhibaatadu saameysey.

Macluumaad dheeraad ah oo ku saabsan dib u celinta waxaa laga heli karaa Website-ka FDA.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto:                 LEVETIRACETAM 100mg / mL
Lambarka NDC:                  54838054880
Lambarada Lot:                    2190A, 2191A
Taariikhda uu dhacayo:              07/2021

10/14/2019, Pfizer Inc. waxay dib uxasuusatay kiniiniyada Relpax 40mg sababo la xiriira faddaraynta microbial ee alaabada aan nadiifka ahayn. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray dib u soo celinta daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u celinta waxaa laga heli karaa Website-ka FDA. 

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto:                 Kiniiniga Relpax 40mg
Lambarka NDC:                  0049-2340-45, 0049-2340-05
Lambarada Lot:                   AR5407, CD4565
Taariikhda uu dhacayo:              02/22

09/23/2019, SANDOZ waxay dib uxasuusatay RANITIDINE HCL sababo laxiriira jiritaanka wasakh. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray soocelin heer labaad ah oo ku saabsan dawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u celinta waxaa laga heli karaa Website-ka FDA. 

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto:                 Ranitidine 150mg iyo Ranitidine 300mg
Lambarka NDC:                  00781285560, 00781286531
Lambarada Lot:                  HD8625, HD9275, HU2207, HX6676, HX6677, HC9266, HD1865, HP9441, JK7994, JK8659, HD1862, HP9438, HP9439, HP9440
Taariikhda uu dhacayo:             4/30/2020, 4/30/2020, 8/31/2020, 3/31/2021, 3/31/2021, 4/30/2020, 4/30/2020, 9/30/2020, 8/31/2021, 8/31/2021, 4/30/2020, 9/30/2020, 9/30/2020, 9/30/2020

9/19/2019, Torrent Pharma, Inc., waxay dib uxasuusatay Losartan Potassium (dhamaan awooda) iyo Losartan Potassium / Hydrochlorothiazide (dhamaan awooda) sababtoo ah jiritaanka wasakh. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray Fasalka II ee daawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u celinta waxaa laga heli karaa Website-ka FDA. 

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto:                 Losartan Potassium iyo Losartan Potassium / Hydrochlorothiazide
Lambarka NDC:                  13668-409-10, 13668-115-90, 13668-115-10, 13668-116-90, 13668-118-90
Lambarada Lot:                  4DU2E009, 4DU3E009, 4DU3D018, BEF7D051, 4P04D007
Taariikhda uu dhacayo:             12/31/2020, 02/28/2021

Markay ahayd 7/16/2019, Bionpharma, Inc. waxay dib uxasuusatay Clobazam Oral Suspension 2.5mg / mL sababo laxiriira natiijooyinka qeexitaan la'aanta ee Imtixaanada Tirakoobka Microbial. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray soocelin heer labaad ah oo ku saabsan dawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u celinta waxaa laga heli karaa Websaydhada FDA.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto:                 Clobazam Cayrinta Afka 2.5mg / mL
Lambarka NDC:                  69452-116-45
Lambarada Lot:                  18246
Taariikhda uu dhacayo:             09/2020

Markay ahayd 07/11/2019, Tris Pharma, Inc. waxay dib uxasuusatay Hydrocodone / Chlorpheniramine 10 / 8mg / 5mL awood qaldan darteed. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray soocelin heer labaad ah oo ku saabsan dawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u celinta waxaa laga heli karaa Websaydhada FDA.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto:                 Hydrocodone / Chlorpheniramine 10 / 8mg / 5mL
Lambarka NDC:                  27808-086-02
Lambarada Lot:                  14079
Taariikhda uu dhacayo:             10/2021 

5/3/2019, Heritage Pharmaceuticals Inc. iyo Torrent Pharma Inc. waxay dib uxasuusteen Losartan 25mg, 50mg, 100mg Kiniinno sababo la xiriira jiritaanka wasakh. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray Fasaxii Xusuus-darrada II ee daawooyinka ay dhibaatadu saameysey.

2/28/2019, Camber Pharmaceuticals Inc. waxay dib uxasuusatay Losartan 25mg, 50mg, kiniiniyada 100mg sababo la xiriira jiritaanka wasakh. Maamulka Cunnada iyo Dawooyinka ee Maraykanka (FDA) ayaa soo saaray Fasax Xusuus-tir ah oo ah dawooyinka ay saamaysay.

4/10/2019, Torrent Pharma, Inc. waxay dib uxasuusatay kiniiniyada loo yaqaan 'Losartan potassium potassium' sababtoo ah jiritaanka wasakh. Maamulka Cuntada iyo Dawooyinka ee Maraykanka (FDA) ayaa soo saaray Fasaxii Xusuusta II ee dawooyinka ay dhibaatadu soo gaadhay.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=171978

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: Losartan 25mg, 50mg, 100 mg kiniin | Kiniiniyada loo yaqaan 'Losartan Potassium Tablets' (dhamaan awooda) 

Nambarada NDC: 31722070010, 31722070130, 31722070290
Lambarro badan: Sababtoo ah mugga badan ee lambarrada badan ee la saameeyay, fadlan tixraac bogga shabakadda FDA ee kor ku xusan si aad u hesho macluumaad gaar ah oo ku saabsan tirada badan ee la xiriirta daawadaada.

4/25/2019, Zydus Pharmaceuticals waxay dib uxasuusatay kiniiniyada Acyclovir 400mg sababo la xiriira iskudhafka kiniinka. Maamulka Cunnada iyo Dawooyinka ee Maraykanka (FDA) ayaa soo saaray Fasax Xusuus-tir ah oo ah dawooyinka ay saamaysay.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=172494

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto:  Acyclovir 400mg kiniinno, 100 dhalooyin tirinta
Lambarka NDC:  68382079101
Lambarro badan: Z804517
Taariikhda uu dhacayo: 11/30/2020

Markay ahayd 4/19/2019, Alvogen, Inc waxay dib uxasuusatay Fentanyl 12mcg / hr dhejisyo transdermal sababo laxiriira isku-darka baakadaha oo keenaya awood qaldan oo kujirta sanduuqyada. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray Fasalka Xusuusta I ee dawooyinka ay saameeyeen.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=172322

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: Fentanyl 12mcg / hr transdermal patch
Lambarka NDC: 47781042347
Lambarro badan iyo taariikhda uu dhacayo: Luudh #: 180060, Exp 05/2020; 180073, Baahi 06/2020.

3/1/2019, Apotex Inc. waxay dib uxasuusatay Kiniiniyada Drospirenone iyo Ethinyl Estradiol 3mg / 0.03mg sababo laxiriira kiniin iskujir ah. Maamulka Cunnada iyo Dawooyinka ee Maraykanka (FDA) ayaa soo saaray Fasax Xusuus-tir ah oo ah dawooyinka ay saamaysay.

Macluumaad dheeraad ah oo ku saabsan dib u celinta waxaa laga heli karaa Website-ka FDA. 

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto:                 Kiniiniyada Drospirenone iyo Ethinyl Estradiol 3mg / 0.03mg
Lambarka NDC:                  60505418303
Lambarada Lot:                  7DY008A, 7DY009A, 7DY010A, 7DY011A
Taariikhda uu dhacayo:             08/2020 

1/18/2019, Prinston Pharmaceutical Inc. waxay dib uxasuusatay Kiniiniyada Irbesartan 300mg sababo la xiriira jiritaanka wasakh. Maamulka Cunnada iyo Dawooyinka ee Maraykanka (FDA) ayaa soo saaray Fasax Xusuus-tir ah oo ah dawooyinka ay saamaysay.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=170280

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: Kiniiniyada Irbesartan 300mg
Lambarka NDC: 43547-376-09
Lambarada Lot: 331B18009

Bishii Nofeembar 14, 2018, ASCEND SHAQAALAHA waxay dib u soo celiyeen QUETIAPINE FUMARATE 400 MG sababo la xiriira joogitaanka walax shisheeye. Maamulka Cunnada iyo Dawooyinka ee Maraykanka (FDA) ayaa soo saaray Fasax Xusuus-tir ah oo ah dawooyinka ay saamaysay. Tani waa soo noqoshada dawada FDA ee socota.

Dawada la xasuusto: Quetiapine Fumarate 400 mg

Lambarka NDC: 67877024801

Lambarka Naadiga: 7143908

Taariikhda uu dhacayo: November 2020

Markay ahayd 1/18/2019, Aurobindo Pharma USA Inc. waxay dib uxasuusatay Valsartan 160mg, 320mg, 40mg, kiniiniyada 80mg sababo la xiriira jiritaanka wasakh. Maamulka Cunnada iyo Dawooyinka ee Maraykanka (FDA) ayaa soo saaray Fasax Xusuus-tir ah oo ah dawooyinka ay saamaysay.

Bishii Nofeembar 20, 2018 Mylan wuxuu dib uxasuustay Amlodipine-Valsartan & Valsartan sababo laxiriira raadadka xadiga sunta nijaasta NDEA (N-Nitrosodiethylamine) ee laga helay maaddada dawada firfircoon ee Valsartan. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray Fasaxii Xusuus-darrada II ee daawooyinka ay dhibaatadu saameysey.

Macluumaad dheeraad ah oo ku saabsan dib u celinta waxaa laga heli karaa Website-ka FDA. 

Dawada la xasuusto: 

• Valsartan 40 mg, 60 mg, 80 mg, 160 mg, iyo 320 mg
• Amlodipine-Valsartan 5/160 mg, 10/160 mg iyo 10/320 mg
• Valsartan-Hydrochlorathiazide 320/25 MG 

Lambarka NDC: 65862057290, 65862057390, 65862057030, 65862057190, 00378-1721-93, 00378-1722-93, 00378-1724-93, 00378-5813-77, 00378-5814-77, 00378-5807-93, 0378-5815-77 and 0378-6325-05

Lambarka Naadiga: 3079500, 3061986, 3079709, 3077618, 3079708, 3063782, 3071352, 3061169, 3081499, 3080009, 3080010, 3079205, 3084886, 3093804

Taariikhda uu dhacayo:  Nofeembar 2018, Janaayo 2019, Maarso 2019, Luulyo 2019, Nofeembar 2019, Diseembar 2019, Janaayo 2020, Febraayo 2020, Maarso 2020

09/04/2018, Dr. Reddy's Lab wuxuu dib uxasuustey Tizanidine HCL 2 MG sababo laxiriira kiniinka. Kiniiniyada Glimepiride waxaa laga helay dhalooyinka Tizanidine. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray Fasaxii Xusuusta II ee daawada ay dhibaatadu saameysey.  

Dawada la xasuusto: Tizanidine HCL 2 mg

Lambarka NDC: 55111017915

Lambarada Lot: T800304

Taariikhda uu dhacayo: 03/2021

Bishii Janaayo 4, 2018, Pfizer Inc. waxay dib u soo celisay Diphenoxylate iyo Atropine 2.5 mg / 0.025mg (NDC # 59762-1061-01 iyo 59762-1061-02) sababo la xiriira kala duwanaanshaha miisaanka ee keena kiniiniyada oo ah xoog aan sax ahayn. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray Fasalka Xusuusta # 1 ee daawooyinka ay dhibaatadu saameysey.

Dawada la xasuusto: Diphenoxylate iyo Atropine 2.5 mg / 0.025mg

Lambarka NDC: 59762-1061-01 and 59762-1061-02

Lambarka Naadiga: R83962, R93347, R93348, R93349, R93350, R93351, R93352, R93356, R93357, R93358, R97310, S57831, S57832, S57834

Taariikhda uu dhacayo: 2021 OCT 31, 2021 NOV 30

Markay ahayd 05/31/2018, Apotex Corp waxay dib uxasuusatay Fluticasone 50mcg sababo laxiriira jiritaanka waxyaalo iskudarsan iyo kuwa dabacsan oo kujira daawada. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray Fasalka 2-aad oo dib loogu soo celinayo daawooyinka ay saameysay.

Dawada lagu xasuustoFluticasone 50mcg

Lambarka NDC: 60505-0829-01

Lambarka Naadiga: NJ4501

Taariikhda uu dhacayo: 07/2020

Bishii Janaayo 4, 2018, Pfizer Inc. waxay dib u soo celisay Diphenoxylate iyo Atropine 2.5 mg / 0.025mg (NDC # 59762-1061-01 iyo 59762-1061-02) sababo la xiriira kala duwanaanshaha miisaanka ee keena kiniiniyada oo ah xoog aan sax ahayn. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray Fasalka Xusuusta # 1 ee daawooyinka ay dhibaatadu saameysey.

Macluumaad dheeraad ah oo ku saabsan dib u soo celinta waxay ku taal: http://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Macluumaadka faahfaahsan ee badeecada dib loo soo celiyey ayaa hoos ku taxan:

Dawada la xasuusto: Diphenoxylate iyo Atropine 2.5 mg / 0.025mg

Lambarka NDC: 59762-1061-01 and 59762-1061-02

Lambarka Luuqada: R83962, R93347, R93348, R93349, R93350, R93351, R93352, R93356, R93357, R93358, R97310, S57831, S57832, S57834

Taariikhda uu dhacayo: Oktoobar 31, 2021, Nofeembar 30, 2021