Warbixinta Dib U Xusuusashada Daroogada

Sida February 2026, dib u soo celinta daroogada ayaa halkan lagu soo dhejin doonaa dhammaan qorshayaasha caafimaadka ee CHPW. Haddii aad rabto inaad aragto dib u soo celinta hore ee qorshayaashayada Medicare Advantage ama Shakhsi ahaaneed & Qoyska, fadlan eeg boggaga dib u soo celinta daroogada:

Medicare Advantage Shakhsi & Qoyska

Warbixinta Dib u Celinta Daawada waa daawooyinka dhakhtarku qoro ee dhawaan ay soo saartay Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA). Waa kan waxa aad sameyneyso haddii daawooyinka laguu qoray dib loo soo celiyo:

Haddii aad qabto daawo ay saameysay dib u soo celinta

La xidhiidh farmashiistahaaga iyo bixiyahaaga.
Xaqiiji haddii lambarka booska aad heshay uu qayb ka yahay soo celintan iyo tilmaamo dheeraad ah.
La xiriir adeeg bixiyahaaga ama farmashiistahaaga haddii aad dareento wax dareen celin ah.
Ka hubi sumadda daawada ee lambarkaaga badan ee daroogada iyo taariikhda uu dhacayo si aad u ogaato haddii mid ka mid ah daawooyinkaaga ay saameyn ku leedahay soo celinta.
Haddii aad daawada leedahay, la xiriir farmasiga aad ka heshay. Ficil kastoo xun ama dhacdooyin ka yimaada isticmaalka daawooyinka laguu qoro waa in lagu soo wargeliyaa FDA halkan ama wacayo 1-800-FDA-0178.

La soco ogeysiisyada soo celinta ee hadda jira adigoo booqanaya Website-ka FDA.

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

Daawooyinka 2026 ee la soo celiyey

LEVOTHYROXINE SODIUM 150 MCG

On 1/21/2026, ALVOGEN, INC waxay dib u soo celisay LEVOTHYROXINE SODIUM 150 MCG sababtoo ah Isku-dhafka Badeecada: Hal dhalo oo ka mid ah qaybtan ayaa farmashiyuhu ku sheegay inay ku jirto 88 kiniin oo mcg ah halkii ay ka ahaan lahayd 150 kiniin oo mcg ah. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray Dib u Celinta Heerka II ee daawooyinka ay saameysay.

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

Dawada la xasuusto: LEVOTHYROXINE SODIUM 150 MCG
Lambarka NDC: 47781066210
Nambarka (tirada): MHA21825
Taariikhda (yada) uu Dhacayo: 12/31/2027

Maxaa la sameeyaa ➜

FUROSEMIDE 40 MG

On 01/28/2026, RISING PHARM waxay dib u soo celisay FUROSEMIDE 40 MG sababtoo ah joogitaanka walax shisheeye. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray Dib u Celinta Heerka II ee daawooyinka ay saameysay.

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

Dawada la xasuusto: FUROSEMIDE 40 MG
Lambarka NDC: 64980056310
Nambarka (tirada): FUB125042G
Taariikhda (yada) uu Dhacayo: 05/13/2027

Maxaa la sameeyaa ➜

OXYCODONE-ACETAMINOPHEN 7.5-325 MG

On 01/14/2026, MALLINCKRODT waxay dib u soo celisay OXYCODONE-ACETAMINOPHEN 7.5-325 MG sababtoo ah Tilmaamaha Kiniiniga/Kaabsulka oo fashilmay: Waxaa jira suurtogalnimo ah in calaamaddu ka maqan tahay kiniiniyada. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray Dib u Celinta Heerka II ee daawooyinka ay saameysay.

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

Dawada la xasuusto: OXYCODONE-ACETAMINOPHEN 7.5-325 MG
Lambarka NDC: 00406052201
Nambarka (tirada): 0522J23493
Taariikhda (yada) uu Dhacayo: 03/2027

Maxaa la sameeyaa ➜

OXYCODONE-ACETAMINOPHEN 10MG-325MG

On 01/14/2026, MALLINCKRODT waxay dib u soo celisay OXYCODONE-ACETAMINOPHEN 10MG-325MG sababtoo ah Tilmaamaha Kiniiniga/Kaabsulka oo fashilmay: Waxaa jira suurtogalnimo ah in calaamaddu ka maqan tahay kiniiniyada. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray Dib u Celinta Heerka II ee daawooyinka ay saameysay.

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

Dawada la xasuusto: OXYCODONE-ACETAMINOPHEN 10MG-325MG
Lambarka NDC: 00406052301
Nambarka (tirada): 0523J23904, 0523J24426, 0523J24427
Taariikhda (yada) uu Dhacayo: 05 / 2027, 06 / 2027

Maxaa la sameeyaa ➜

WEGOVY 0.5MG/.5ML

On 01/07/2026, Novo Nordisk waxay dib u soo celisay WEGOVY 0.5MG/.5ML sababtoo ah Jiritaanka Walax Walax ah: Timaha ayaa laga helay irbad hore loo buuxiyay. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray Dib u Celinta Heerka II ee daawooyinka ay saameysay.

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

Dawada la xasuusto: WEGOVY 0.5MG/.5ML
Lambarka NDC: 00169450514
Nambarka (tirada): RZFHD52, RZFHW93
Taariikhda (yada) uu Dhacayo: 10/31/2026

Maxaa la sameeyaa ➜

WEGOVY 1 MG/0.5ML

On 01/07/2026, Novo Nordisk waxay dib u soo celisay WEGOVY 1 MG/0.5ML sababtoo ah Jiritaanka Walax Walax ah: Timaha ayaa laga helay irbad hore loo buuxiyay. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray Dib u Celinta Heerka II ee daawooyinka ay saameysay.

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

Dawada la xasuusto: WEGOVY 1 MG/0.5ML
Lambarka NDC: 00169450114
Nambarka (tirada): RZFYK06, RZFYA53
Taariikhda (yada) uu Dhacayo: 3/31/2027

Maxaa la sameeyaa ➜

Kaydka: 2025 Daawooyinka La Soo Celiyay

LISDEXAMFETAMINE DIMESYLATE 70 MG

On 11/05/2025, SUN PHARMACEUTICAL dib loogu yeero LISDEXAMFETAMINE DIMESYLATE 70 MG sababtuna tahay Tilmaamaha Falalka Fashilmay: Natiijooyin aan qeexnayn oo lagu arkay tijaabada kala dirida inta lagu jiro falanqaynta 12-bilood ee saldhiga xasiloonida muddada dheer (25°C, 60% RH) ee Lisdexamfetamine dimesylate capsulate. 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: LISDEXAMFETAMINE DIMESYLATE 70 MG
Nambarka NDC: 57664005288
Lambarka Luuqada: AD48712, AD50898
Taariikhda uu dhacayo: 04/30/2026, 05/31/2026

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.

LISDEXAMFETAMINE DIMESYLATE 60 MG

On 11/05/2025, SUN PHARMACEUTICAL dib loogu yeero LISDEXAMFETAMINE DIMESYLATE 60 MG sababtuna tahay Tilmaamaha Falalka Fashilmay: Natiijooyin aan qeexnayn oo lagu arkay tijaabada kala dirida inta lagu jiro falanqaynta 12-bilood ee saldhiga xasilloonida muddada dheer (25°C, 60% RH)
Lisdexamfetamine dimesylate capsules. 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: LISDEXAMFETAMINE DIMESYLATE 60 MG
Nambarka NDC: 57664005188
Lambarka Naadiga: AD48711, AD50896
Taariikhda uu dhacayo: 04/30/2026, 05/31/2026

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.

LISDEXAMFETAMINE DIMESYLATE 50 MG

On 11/05/2025, SUN PHARMACEUTICAL dib loogu yeero LISDEXAMFETAMINE DIMESYLATE 50 MG sababtuna tahay Tilmaamaha Falalka Fashilmay: Natiijooyin aan qeexnayn oo lagu arkay tijaabada kala dirida inta lagu jiro falanqaynta 12-bilood ee saldhiga xasilloonida muddada dheer (25°C, 60% RH)
Lisdexamfetamine dimesylate capsules. 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 lagu xasuusto: LISDEXAMFETAMINE DIMESYLATE 50 MG
Lambarka NDC: 57664005088
Lambarka Luuqada: AD48710, AD50895
Taariikhda uu dhacayo: 04/30/2026, 05/31/2026

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.

LISDEXAMFETAMINE DIMESYLATE 40 MG

On 11/05/2025, SUN PHARMACEUTICAL dib loogu yeero LISDEXAMFETAMINE DIMESYLATE 40 MG sababtuna tahay Tilmaamaha Falalka Fashilmay: Natiijooyin aan qeexnayn oo lagu arkay tijaabada kala dirida inta lagu jiro falanqaynta 12-bilood ee saldhiga xasiloonida muddada dheer (25°C, 60% RH) ee Lisdexamfetamine dimesylate capsulate. 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 lagu xasuusto: LISDEXAMFETAMINE DIMESYLATE 40 MG
Nambarka NDC: 57664004988
Lambarka Luuqada: AD48709, AD50894
Taariikhda uu dhacayo: 04/30/2026, 05/31/2026

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.

LISDEXAMFETAMINE DIMESYLATE 30 MG

On 11/05/2025, SUN PHARMACEUTICAL dib loogu yeero LISDEXAMFETAMINE DIMESYLATE 30 MG sababtuna tahay Tilmaamaha Falalka Fashilmay: Natiijooyin aan qeexnayn oo lagu arkay tijaabada kala dirida inta lagu jiro falanqaynta 12-bilood ee saldhiga xasiloonida muddada dheer (25°C, 60% RH) ee Lisdexamfetamine dimesylate capsulate. 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 lagu xasuusto: LISDEXAMFETAMINE DIMESYLATE 30 MG
Nambarka NDC: 57664004888
Lambarka Luuqada: AD42470, AD48708
Taariikhda uu dhacayo: 02/28/2026, 04/30/2026

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.

LISDEXAMFETAMINE DIMESYLATE 20 MG

On 11/05/2025, SUN PHARMACEUTICAL dib loogu yeero LISDEXAMFETAMINE DIMESYLATE 20 MG sababtuna tahay Tilmaamaha Falalka Fashilmay: Natiijooyin aan qeexnayn oo lagu arkay tijaabada kala dirida inta lagu jiro falanqaynta 12-bilood ee saldhiga xasiloonida muddada dheer (25°C, 60% RH) ee Lisdexamfetamine dimesylate capsulate. 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 lagu xasuusto: LISDEXAMFETAMINE DIMESYLATE 20 MG
Nambarka NDC: 57664004788
Lambarka Luuqada: AD42469, AD48707
Taariikhda uu dhacayo: 02/28/2026, 04/30/2026

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.

LISDEXAMFETAMINE DIMESYLATE 10 MG

On 11/05/2025, SUN PHARMACEUTICAL dib loogu yeero LISDEXAMFETAMINE DIMESYLATE 10 MG sababtuna tahay Tilmaamaha Falalka Fashilmay: Natiijooyin aan qeexnayn oo lagu arkay tijaabada kala dirida inta lagu jiro falanqaynta 12-bilood ee saldhiga xasiloonida muddada dheer (25°C, 60% RH) ee Lisdexamfetamine dimesylate capsulate. 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 lagu xasuusto: LISDEXAMFETAMINE DIMESYLATE 10 MG
Nambarka NDC: 57664004688
Lambarka Luuqada: AD42468, AD48705
Taariikhda uu dhacayo: 02/28/2026, 04/30/2026

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.

DULOXETINE HCL 60 MG

On 11/05/2025, BREKENRIDGE dib loo wacay DULOXETINE HCL 60 MG sababtuna tahay leexleexyada CGMP: N-nitroso-duloxetine wasakh ka saraysa xadka qiimaynta badbaadada ee 12.5ppm. Maamulka Cuntada iyo Dawooyinka ee Maraykanka (FDA) ayaa soo saaray Heerka II Dib u soo celinta daawooyinka 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 lagu xasuusto: DULOXETINE HCL 60 MG
Nambarka NDC: 51991074890, 51991074810
Lambarka Luuqada: 240721C, 230286C
Taariikhda uu dhacayo: 02/28/2027, 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 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.

PRAZOSIN HCL 5 MG

On 11/05/2025, TEVA USA waxay dib u wacday PRAZOSIN HCL 5 MG sababtuna tahay CGMP Deviations-Natiijooyinka Tijaabada ee N-nitroso Prazosin nijaasta C ee ka sarreeya Habka Qaybinta Awoodda Kaansarowga (CPCA) ee la aqbali karo ee xaddidaadda kor ku xusan. The
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: PRAZOSIN HCL 5 MG
Lambarka NDC: 00093406901, 00093406952, 00093406905
Lambarka Naadiga: 3010403A, 3010385A, 3010404A, 3010405A, 3010510A, 3010528A, 3010354A, 3010592A, 3010605A, 3010611A, 3010612A, 3010655A, 3010703A, 3010430A, 3010613A, 3010406A
Taariikhda uu dhacayo: 02/2026, 02/2026, 02/2026, 03/2026, 03/2026, 03/2026, 03/2026, 08/2026, 08/2026, 08/2026, 08/2026, 02/2027, 02/2027, 11/2025, 08/2026, 02/2026

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.

BUPROPION XL 300 MG

On 10/29/2025, PHARMACEUTICALS GRAVITI ayaa dib loo celiyay BUPROPION XL 300 MG sababtoo ah Tilmaamaha Kiniinka/Kaabsulaha 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: BUPROPION XL 300 MG
Lambarka NDC: 16571086303
Lambarka Naadiga: BPB124341A
Taariikhda uu dhacayo: 10/2026

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.

PRAZOSIN HCL 2 MG

On 11/05/2025, TEVA PHARMACEUTICALS waxa dib loogu yeedhay PRAZOSIN HCL 2 MG sababtuna tahay leexleexyada CGMP-natiijooyinka Tijaabada N-nitroso Prazosin nijaasta C ee ka sarraysa Habka Kala soocida Awooda Kansarka (CPCA) ee la aqbali karo ee xadaynta kor ku xusan.

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: PRAZOSIN HCL 2 MG
Lambarka NDC: 00093406801, 00093406810
Lambarka Naadiga: 3010398A, 3010399A, 3010400A, 3010401A, 3010353A, 3010439A, 3010388A, 3010526A, 3010527A, 3010343A, 3010591 3010352A, 3010468A, 3010469A, 3010461A, 3010629A, 3010653A, 3010654A, 3010679A, 3010702A, 3010402A, 3010547 3010593A, 3010610A
Taariikhda uu dhacayo: 12/2025, 12/2025, 12/2025, 12/2025, 12/2025, 01/2026, 01/2026, 03/2026, 03/2026, 07/2026, 10/2025, 11/2025, 02/2026, 02/2026, 02/2026, 09/2026, 01/2027,02/2027, 02/2027, 02/2027, 04/2026, 02/2028, 07/2026, 09/2026

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.

PRAZOSIN HCL 1 MG

On 11/05/2025, TEVA PHARMACEUTICALS waxa dib loogu yeedhay PRAZOSIN HCL 1 MG sababtuna tahay leexleexyada CGMP-natiijooyinka Tijaabada N-nitroso Prazosin nijaasta C ee ka sarraysa Habka Kala soocida Awooda Kansarka (CPCA) ee la aqbali karo ee xadaynta kor ku xusan.

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: PRAZOSIN HCL 1 MG
Lambarka NDC: 00093406701, 00093406710
Lambarka Naadiga: 3010544A, 3010545A, 3010567A, 3010590A, 3010601A, 3010602A, 3010603A, 3010652A, 3010670A, 3010678A, 3010671 3010700A, 3010701A, 3010440A, 3010672A
Taariikhda uu dhacayo: 10/2025, 10/2025, 12/2025, 02/2026, 03/2026, 03/2026, 03/2026, 07/2026, 07/2026, 07/2026, 08/2026, 08/2026, 08/2026, 12/2025, 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 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.

LEVOTHYROXINE SODIUM 88 MCG

On 10/15/2025, ACCORD HEALTHCARE waxa dib loogu yeedhay LEVOTHYROXINE SODIUM 88 MCG sababtuna tahay Awood-hoosaad: Inta lagu jiro tijaabada xasiloonida muddada dheer ee Levothyroxine Sodium Tablets USP ee 88 mcg, nuxurka qiimaynta ayaa lagu arkay ka hooseeya heerka qeexitaanka la ansixiyay. 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: 16729045015
Lambarka Naadiga: D2300045
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 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.

KETROLAC TROMETAMINE 0.5 %

On 10/08/2025, APOTEX CORP waxay dib u soo celisay KETOROLAC TROMETHAMINE 0.5 % iyadoo ay ugu wacan tahay Xaqiijinta Madhalaysnimada; Miisaan aan caadi ahayn oo luma sababtoo ah xirid dhalada oo aan habboonayn taasoo horseedaysa walaacyo dhalmo la'aan. Maamulka Cuntada iyo Dawooyinka ee Maraykanka (FDA) ayaa soo saaray fasal
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: KETROLAC TROMETAMINE 0.5 %
Lambarka NDC: 60505100301
Lambarka Naadiga: VA0444, VA4608 iyo TZ7016
Taariikhda uu dhacayo: 01/2026, 01/2026 iyo 12/2025

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.

ARIPIPRAZOLE 10 MG

On 09/24/2025, ASCEND LABORATORIES LLC dib loo wacay ARIPIPRAZOLE 10 MG daawadii ugu awooda badnayd 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: ARIPIPRAZOLE 10 MG
Lambarka NDC: 67877043203
Lambarka Naadiga: 24144162
Taariikhda uu dhacayo: 09/2027

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.

CYCLOBENZAPRINE HCL 10 MG

On 09/24/2025, UNICHEM PHARMA waxay dib u wacday CYCLOBENZAPRINE HCL 10 MG iyadoo ay ugu wacan tahay Summadaynta: Calaamadaynta Isku-darka; Dhalooyinka Meloxicam USP, 7.5mg, kiniinnada 90-count (midabka jaalaha ah), ayaa lagu calaamadeeyay sida Cyclobenzaprine Hydrochloride Tablets USP, 10 mg 90-count tablets (buluug
color) Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Heerka I 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: CYCLOBENZAPRINE HCL 10 MG
Lambarka NDC: 29300041519
Lambarka Naadiga: GMML24026A
Taariikhda uu dhacayo: 09/30/2027

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.

BELSOMRA 10 MG

On 08/20/2025, MERCK & CO. INC waxay dib u waceen BELSOMRA 10 MG iyadoo ay ugu wacan tahay Tilmaamaha Falalka Fashilmay: suurtagalnimada daahitaanka kala dirida qiyaasta ka dib maamulka taasoo keeni karta daahinta sii deynta daawada, dib u dhigista bilawga hurdada. 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: BELSOMRA 10 MG
Lambarka NDC: 00006003330
Lambarka Naadiga: 2090019 iyo 2123744
Taariikhda uu dhacayo: 04/30/2027

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 booqashada www.fda.gov/medwatch/report.htm ama wac 1-800-FDA-0178.

CINACALCET HCL 90 MG

On 08/06/2025, NOSTRUM LABORATORIES dib ayaa loo yeedhay CINACALCET HCL 90 MG sababtuna tahay Tilmaamaha 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: CINACALCET HCL 90 MG
Lambarka NDC: 64380088504
Lambarka Naadiga: 7715893A
Taariikhda uu dhacayo: 12/31/2027

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.

DOXEPIN HCL 10 MG

On 08/13/2025, ALEMBIC PHARMACEUTICALS ayaa dib loo wacay DOXEPIN HCL 10 MG sababtuna tahay leexashada CGMP: Jiritaanka Walaxda Daroogada Nitrosamine ee ka saraysa xadka ku meel gaarka ah ee la soo jeediyay. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Fasalka II
Dib u xasuusashada dawooyinka ay dhibaatadu saameysey.

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: DOXEPIN HCL 10 MG
Lambarka NDC: 62332063731
Lambarka Naadiga: 23050515142
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.

SPIRONOLACTONE 25 MG

On 08/13/2025, SUN PHARMACEUTICAL dib loogu yeero SPIRONOLACTONE 25 MG iyadoo ay ugu wacan tahay Jiritaanka walxaha shisheeye: loo aqoonsaday sida aluminium. 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: SPIRONOLACTONE 25 MG
Lambarka NDC: 53489014301
Lambarka Naadiga: P3314
Taariikhda uu dhacayo: 11/30/2026

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.

SUCRALFATE 1 G

On 08/06/2025, NOSTRUM LABORATORIES dib loo soo celiyay SUCRALFATE 1 G sababo la xiriira leexinta CGMP: Shirkadda dib u soo celinta ayaa lagu xareeyay cutubka 11 ee Sebtembar 2024. Natiijo ahaan, ma kormeeri karto barnaamijka tayada leh oo markaa ma xaqiijin karto in alaabtu ay la kulanto aqoonsiga, xoogga, tayada, iyo sifooyinka daahirsanaanta in ay yihiin kuwo la sheegayo ama loo soo bandhigay inay leeyihiin, la siiyay alaabada. 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: SUCRALFATE 1 G
Lambarka NDC: 29033000305
Lambarka Naadiga: Wax badan
Taariikhda uu dhacayo: Dhammaan Taariikhaha uu dhacayo

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.

RIZATRIPTAN 5 MG

On 07/23/2025, ASCEND LABORATORIES dib loo wacay RIZATRIPTAN 5 MG sababtuna tahay CGMP Weecan: ogaanshaha N-nitroso-dimethyl-rizatriptan wasakh, ka sarreeya FDA waxay ku talisay xadka la aqbali karo. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Fasalka II
Dib u xasuusashada dawooyinka ay dhibaatadu saameysey.

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 5 MG
Lambarka NDC: 67877026118
Lambarka Naadiga: 23142117, 23142119, 23142122
Taariikhda uu dhacayo: May 2026 iyo Juun 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.

RIZATRIPTAN 10 MG

On 07/23/2025, ASCEND LABORATORIES dib loo wacay RIZATRIPTAN 10 MG sababtuna tahay CGMP Weecan: ogaanshaha N-nitroso-dimethyl-rizatriptan wasakh, ka sarreeya FDA waxay ku talisay xadka la aqbali karo. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Fasalka II
Dib u xasuusashada dawooyinka ay dhibaatadu saameysey.

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 10 MG
Lambarka NDC: 67877026218
Lambarka Naadiga: 22143653, 22143675, 22144528, 22144977, 23140257, 23140999, 23141900, 23142118, 23142120, 23142123, 23144563, 23144565, 24142623, 24142624, 24142626, 24143469
Taariikhda uu dhacayo: Luulyo 2025, Sebtembar 2025, Noofambar 2025, Diseembar 2025, Feb 2026, Meey 2026, Noofambar 2026, Meey 2027, Juun 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.

LISDEXAMFETAMINE DIMESYLATE 60 MG

On 07/23/2025, SUN PHARMACEUTICAL dib loogu yeero LISDEXAMFETAMINE DIMESYLATE 60 MG sababtuna tahay Tilmaamaha Falalka Fashilmay: Natiijooyin qeexid ka baxsan oo lagu arkay tijaabada kala dirida inta lagu jiro falanqaynta 9 bilood ee xasilloonida muddada dheer (25Â¿C, 60% RH). The
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 lagu xasuusto: LISDEXAMFETAMINE DIMESYLATE 60 MG
Lambarka NDC: 57664005188
Lambarka Naadiga: AD42648
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 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.

LEVOTHYROXINE SODIUM 50 MCG

On 07/23/2025, ACCORD HEALTHCARE waxa dib loogu yeedhay LEVOTHYROXINE SODIUM 50 MCG sababtoo ah Dawooyinka Awood-hoosaadka ah: Qiimaynta hoos tilmaanta la ansixiyay. 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
Nambarka NDC: 16729044815
Lambarka Naadiga: D2300087
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 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.

LEVOTHYROXINE SODIUM 25 MCG

On 07/23/2025, ACCORD HEALTHCARE waxa dib loogu yeedhay LEVOTHYROXINE SODIUM 25 MCG sababtoo ah Dawooyinka Awood-hoosaadka ah: Qiimaynta hoos tilmaanta la ansixiyay. 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 lagu xasuusto: LEVOTHYROXINE SODIUM 25 MCG
Lambarka NDC: 16729044717
Lambarka Naadiga: D2400679
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 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.

LEVOTHYROXINE SODIUM 25 MCG

on 07/23/2025, ACCORD HEALTHCARE waxa dib loogu yeedhay LEVOTHYROXINE SODIUM 25 MCG sababtoo ah Dawooyinka Awood-hoosaadka ah: Qiimaynta hoos tilmaanta la ansixiyay. 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 lagu xasuusto: LEVOTHYROXINE SODIUM 25 MCG
Nambarka NDC: 16729044715
Lambarka Naadiga: D2300325, D2400536
Taariikhda uu dhacayo: 01/31/2026, 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 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.

LEVOTHYROXINE SODIUM 175 MCG

On 07/23/2025, ACCORD HEALTHCARE waxa dib loogu yeedhay LEVOTHYROXINE SODIUM 175 MCG sababtoo ah Dawooyinka Awood-hoosaadka ah: Qiimaynta hoos tilmaanta la ansixiyay. 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 175 MCG
Lambarka NDC: 16729045617
Lambarka Naadiga: D2300042
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 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.

LEVOTHYROXINE SODIUM 150 MCG

On 07/23/2025, ACCORD HEALTHCARE waxa dib loogu yeedhay LEVOTHYROXINE SODIUM 150 MCG sababtoo ah Dawooyinka Awood-hoosaadka ah: Qiimaynta hoos tilmaanta la ansixiyay. 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 150 MCG
Lambarka NDC: 16729045517
Lambarka Naadiga: D2300076
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 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.

LEVOTHYROXINE SODIUM 112 MCG

On 07/23/2025, ACCORD HEALTHCARE waxa dib loogu yeedhay LEVOTHYROXINE SODIUM 112 MCG sababtoo ah Dawooyinka Awood-hoosaadka ah: Qiimaynta hoos tilmaanta la ansixiyay. 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 112 MCG
Lambarka NDC: 16729045217
Lambarka Naadiga: D2300104
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 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.

LEVOTHYROXINE SODIUM 100 MCG

on 07/23/2025, ACCORD HEALTHCARE waxa dib loogu yeedhay LEVOTHYROXINE SODIUM 100 MCG sababtoo ah Dawooyinka Awood-hoosaadka ah: Qiimaynta hoos tilmaanta la ansixiyay. 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 100 MCG
Lambarka NDC: 16729045117
Lambarka Naadiga: D2300092, D2400722
Taariikhda uu dhacayo: 12/31/2025, 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 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.

GABAPENTIN 100 MG

On 07/09/2025, FARMAAJO WEYN ayaa dib u celiyay GABAPENTIN 100 MG weel cilladaysan awgeed; baakadaha finanka si aan ku filneyn loo xirin. 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 100 MG
Lambarka NDC: 00904666561
Lambarka Naadiga: M05205
Taariikhda uu dhacayo: 10 / 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.

METOPROLOL SUCCINATE 25 MG

On 07/09/2025, GRANULES PHARMA waxa dib loogu yeedhay METOPROLOL SUCCINATE 25 MG sababtuna tahay Tilmaamaha Falalka Fashilan: Alaabtu waxay ku guuldareysatay inay buuxiso shuruudaha aqbalaada kala dirida daraasadaha xasiloonida ee bisha 6th (25C/60% RH) 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: METOPROLOL SUCCINATE 25 MG
Lambarka NDC: 70010078001
Lambarka Naadiga: 1400008A
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 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.

METOPROLOL SUCCINATE 25 MG

On 07/09/2025, GRANULES PHARMA waxa dib loogu yeedhay METOPROLOL SUCCINATE 25 MG sababtuna tahay Tilmaamaha Falalka Fashilan: Alaabtu waxay ku guuldareysatay inay buuxiso shuruudaha aqbalaada kala dirida daraasadaha xasiloonida ee bisha 6th (25/60% RH) 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: METOPROLOL SUCCINATE 25 MG
Lambarka NDC: 70010078005
Lambarka Naadiga: 1400008B
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 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.

METOCLOPRAMIDE HCL 10 MG

On 07/02/2025, TEVA PHARMACEUTICALS waxay dib u wacday METOCLOPRAMIDE HCL 10 MG iyadoo ay ugu wacan tahay Joogitaanka kiniiniyada/kaabsal shisheeye. 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: METOCLOPRAMIDE HCL 10 MG
Lambarka NDC: 00093220301
Lambarka Naadiga: 5420094
Taariikhda uu dhacayo: 09/30/2027

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.

KETROLAC TROMETAMINE 0.5 %

On 07/02/2025, APOTEX CORP waxay dib u soo celisay KETOROLAC TROMETHAMINE 0.5 % taas oo ay ugu wacan tahay Xaqiijinta Madhalaysnimada. 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: KETROLAC TROMETAMINE 0.5 %
Lambarka NDC: 60505100302
Lambarka Naadiga: TZ1236
Taariikhda uu dhacayo: 11/30/2025

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.

AZELASTINE HCL 0.05 %

On 07/02/2025, APOTEX CORP waxay dib u wacday AZELASTINE HCL 0.05 % iyadoo ay ugu wacan tahay Xaqiijinta Madhalaysnimada. 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 lagu xasuusto: AZELASTINE HCL 0.05 %
Nambarka NDC: 60505057804
Lambarka Luuqada: VD1654
Taariikhda uu dhacayo: 06/30/2027

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.

INDOMETHACIN ER 75 MG

On 05/28/2025, KVK TECH waxay dib u xasuusisay INDOMETHACIN ER 75 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 lagu xasuustoINDOMETHACIN ER 75 MG
Nambarka NDC: 10702001601
Lambarka Luuqada: 18400A
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 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.

CARVEDILOL 6.25 MG

On 06/04/2025, GLENMARK PHARMACEUTICALS ayaa dib loo celiyay CARVEDILOL 6.25 MG sababtoo ah leexashada CGMP; Joogitaanka 'N-Nitroso Carvedilol I' wasakh ka sarreeya xadka la aqbali karo ee lagu taliyey. Maamulka Cunnada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saartay Fasalka II
Dib u xasuusashada dawooyinka ay dhibaatadu saameysey.

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 lagu xasuusto: CARVEDILOL 6.25 MG
Nambarka NDC: 68462016305
Lambarka Luuqada19231174, 19231199, 19231164, 19231517,19231527, 19231566, 19231568, 19231595, 19231618, 19231634, 19231638 19231448, 19232043, 19232051, 19232064, 19232322, 19232324, 19232365, 19232380, 19232389, 19232736, 19232743 19232746, 19232756, 19232757, 19233369, 19233371, 19233405, 19233416, 19234162, 19234183, 19234192, 19234204 19234223, 19234243, 19234263, 19234165, 19234242, 19234743, 19234774, 19234993, 19240223, 19240203 19240211, 19240214, 19240247, 19240249, 19240272 iyo 19240319
Taariikhda uu dhacayo: Feb-25, Mar-25, Apr-25, May-25, Jun-25, Jul-25, Sep-25, Nov-25, Dec-25 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 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.

CARVEDILOL 6.25 MG

On 06/04/2025, GLENMARK PHARMACEUTICALS ayaa dib loo celiyay CARVEDILOL 6.25 MG sababtoo ah leexashada CGMP; Joogitaanka 'N-Nitroso Carvedilol I' wasakh ka sarreeya xadka la aqbali karo ee lagu taliyey. 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 lagu xasuusto: CARVEDILOL 6.25 MG
Lambarka NDC: 68462016301
Lambarka Luuqada: 19233369, 19234162 iyo 19240543
Taariikhda uu dhacayo: Jul-25, Sep-25, 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 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.

CARVEDILOL 3.125 MG

On 06/04/2025, GLENMARK PHARMACEUTICALS ayaa dib loo celiyay CARVEDILOL 3.125 MG sababtoo ah leexashada CGMP; Joogitaanka 'N-Nitroso Carvedilol I' wasakh ka sarreeya xadka la aqbali karo ee lagu taliyey. 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 lagu xasuusto: CARVEDILOL 3.125 MG
Lambarka NDC: 68462016205
Lambarka Naadiga: 19231450, 19231464, 19231471, 19231493, 19232083, 19232103, 19232658, 19233328, 19233343, 19233344, 19233345, 19234275,19234843, 19235039, 19240280 iyo 19240296
Taariikhda uu dhacayo: Mar-25, Abriil-25, Juun-25, Jul-25, Sebte-25, Nov-25 iyo Dec-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 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.

CARVEDILOL 3.125 MG

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 3.125 MG
Lambarka NDC: 68462016201
Lambarka Naadiga: 19231450, 19233345, 19234275 iyo 19240280
Taariikhda uu dhacayo: Mar-25, Jul-25, Sep-25 iyo Dec-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 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.

CARVEDILOL 12.5 MG

On 06/04/2025, GLENMARK PHARMACEUTICALS ayaa dib loo celiyay CARVEDILOL 12.5 MG sababtoo ah leexashada CGMP; Joogitaanka 'N-Nitroso Carvedilol I' wasakh ka sarreeya xadka la aqbali karo ee lagu taliyey. 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 lagu xasuusto: CARVEDILOL 12.5 MG
Nambarka NDC: 68462016405
Lambarka Naadiga: 19231899, 19231922, 19231927, 19231967, 19231979, 19232226, 19232234, 19232265, 1923227,19232758, 19232759, 19232762 iyo 19232788
Taariikhda uu dhacayo: Apr-25, May-25 iyo Jun-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 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.

CARVEDILOL 25 MG

On 06/04/2025, GLENMARK PHARMACEUTICALS ayaa dib loo celiyay CARVEDILOL 25 MG sababtoo ah leexashada CGMP; Joogitaanka 'N-Nitroso Carvedilol I' wasakh ka sarreeya xadka la aqbali karo ee lagu taliyey. 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 lagu xasuusto: CARVEDILOL 25 MG
Nambarka NDC: 68462016505
Lambarka Luuqada: 19231107, 19231114, 19231152 iyo 19234866
Taariikhda uu dhacayo: Feb-25 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 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.

AIRSUPRA 90-80 MCG

On 05/28/2025, ASTTRAZENECA waxay dib u wacday AIRSUPRA 90-80 MCG sababtoo ah nidaamka dhalidda cilladaysan. 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 lagu xasuusto: AIRSUPRA 90-80 MCG
Nambarka NDC: 00310908012
Lambarka Naadiga: 6270044C00, 6270040D00, 6270034E00, 6270053C00, 6270045C00, 6270047C00, 6270056C00, 6270052C00, 6270063E00, 6270064C00, 6270071D00, 6270075D00, 6270075F00 and 6270107C00
Taariikhda uu dhacayo: 10/2026, 11/30/2026, 12/31/2026 and 9/30/2027

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.

LEVOTHYROXINE SODIUM 112 MCG

On 05/07/2025, ACCORD HEALTHARE waxa dib loogu yeedhay LEVOTHYROXINE SODIUM 112 MCG sababtoo ah Daawo Awood-hoosaad leh. 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 112 MCG
Lambarka NDC: 16729045215
Lambarka Naadiga: D2400725
Taariikhda uu dhacayo: 03/2026

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.

LEVOTHYROXINE SODIUM 88 MCG

On 05/07/2025, ACCORD HEALTHARE waxa dib loogu yeedhay LEVOTHYROXINE SODIUM 88 MCG sababtoo ah Daawo Awood-hoosaad leh. 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: 16729045017
Lambarka Naadiga: D2300044
Taariikhda uu dhacayo: 12/2025

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.

LEVOTHYROXINE SODIUM 50 MCG

On 05/07/2025, ACCORD HEALTHARE waxa dib loogu yeedhay LEVOTHYROXINE SODIUM 50 MCG sababtoo ah Daawo Awood-hoosaad leh. 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: 16729044817
Lambarka Naadiga: D2400547
Taariikhda uu dhacayo: 02/2026

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.

LEVOTHYROXINE SODIUM 25 MCG

On 05/07/2025, ACCORD CAAFIMAAD, oo la xasuusto LEVOTHYROXINE SODIUM 25 MCG oo ay ugu wacan tahay Dawooyinka Awoodda leh. 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: 16729044717
Lambarka Naadiga: D2300323
Taariikhda uu dhacayo: 01/2026

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.

TESTOSTERONE CYPIONATE 200 MG/ML

On 04/23/2025, EGIA US LLC waxay dib u wacday TESTOSTERONE CYPIONATE 200 MG/ML sababtoo ah cGMP: cabashooyinka kirismaska ee aan dib u milmin xalka ka dib kululaynta iyo ruxitaanka fijaannada. Maamulka Cuntada iyo Dawooyinka ee Mareykanka (FDA) ayaa soo saaray dib u yeerista heerka II ee
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 lagu xasuusto: TESTOSTERONE CYPIONATE 200 MG/ML
Nambarka NDC: 55150027701
Lambarka Luuqada: 1TC24075A
Taariikhda uu dhacayo: 11 / 30 / 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.

CARVEDILOL 12.5 MG

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.

DILTIAZEM 12HR ER 120 MG

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.

HALOPERIDOL DECANOATE 100 MG/ML

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.

LACOSAMIDE 50 MG

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.

LACOSAMIDE 100 MG

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.

LACOSAMIDE 150 MG

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.

LACOSAMIDE 200 MG

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.

GABAPENTIN 600 MG

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.

NITROGLYCERIN 0.3 MG

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.

NITROGLYCERIN 0.4 MG

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.

PRAVASTATIN SODIUM 20 MG (GLENMARK pharmaceuticals)

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.

PRAVASTATIN SODIUM 20 MG (NORTHSTAR RX LLC)

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.

PRAVASTATIN SODIUM 80 MG

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.

PROCHLORPERAZINE MALEATE 10 MG

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.

SAXAGLIPTIN HCL 2.5 MG

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.

SAXAGLIPTIN HCL 5 MG

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.

ROSUVASTATIN CALCIUM 40 MG

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.

SODIUM Kchloride 0.9 %

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.

SOLIFENACIN SUCCINATE 5 MG

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.

SOLIFENACIN SUCCINATE 5 MG

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.

SOLIFENACIN SUCCINATE 10 MG

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.

VENLAFAXINE HCL 75 MG

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.

TESTOSTERONE 25MG (1%)

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.

TESTOSTERONE 50 MG (1%)

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.

LORAZEPAM 2 MG/ML

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.

LORAZEPAM 2 MG/ML

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.

LORAZEPAM INTENSOL 2 MG/ML

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.

FENTANYL 25 MCG/HR

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.

LORAZEPAM 0.5 MG

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.

LORAZEPAM 1 MG

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.

CLONAZEPAM 0.25 MG ODT TABLET

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.

CLONAZEPAM 1 MG ODT TABLET

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.

CLONAZEPAM 2 MG ODT TABLET

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.

LEVOTHYROXINE SODIUM 75 MCG

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.

Warbixinta Dib U Xusuusashada Daroogada

Haddii aad qabto daawo ay saameysay dib u soo celinta

Daawooyinka 2026 ee la soo celiyey

Kaydka: 2025 Daawooyinka La Soo Celiyay

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MA OGEYD...?

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