Warbixinta Dib U Xusuusashada Daroogada

INSULIN GLARGINE-YFGN 100/ML

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

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

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

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

Waxa ay tahay inaad sameyso:

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

HUMALOG 100/ML

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

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

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

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

Waxa ay tahay inaad sameyso:

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

GUDUBKA 0.004 %

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

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

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

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

Waxa ay tahay inaad sameyso:

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

GLYCOPYRRATE 1 MG

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

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

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

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

Waxa ay tahay inaad sameyso:

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

SYMJEPI 0.3MG/0.3

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

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

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

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

Waxa ay tahay inaad sameyso:

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

FIRVANQ 50 MG/ML

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

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

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

Waxa ay tahay inaad sameyso:

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

Qalabka degdegga ah ee GLUCAGON 1 MG

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

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

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

Waxa ay tahay inaad sameyso:

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

METFORMIN HCL ER 750 MG

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

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

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

Waxa ay tahay inaad sameyso:

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

BUSPIRONE HCL 15 MG

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

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

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

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

Waxa ay tahay inaad sameyso:

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

NP THYROID DHAMMAAN XOOGYADA

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

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

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

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

Waxa ay tahay inaad sameyso:

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

HALOPERIDOL DECANOATE 50 MG / ML iyo 100 MG / ML

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

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

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

Waxa ay tahay inaad sameyso:

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

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

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

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

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

Waxa ay tahay inaad sameyso:

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

MAALMAHA DAYTRANA

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

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

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

Waxa ay tahay inaad sameyso:

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

CEFPROZIL 250 MG / 5ML

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

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

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

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

Waxa ay tahay inaad sameyso:

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

GUANFACINE 2 MG ER TABLET

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

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

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

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

Waxa ay tahay inaad sameyso:

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

MOMETASONE DHAQAALAHA 0.1%

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

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

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

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

Waxa ay tahay inaad sameyso:

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

RIOMET 500 MG / 5ML

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

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

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

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

Waxa ay tahay inaad sameyso:

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

DAYTRANA PATCH

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

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

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

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

Waxa ay tahay inaad sameyso:

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

FAMOTIDINE 40 MG FADHIYADA

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

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

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

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

Waxa ay tahay inaad sameyso:

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

IMATINIB MESYLATE 100 MG

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

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

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

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

Waxa ay tahay inaad sameyso:

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

OMEPRAZOLE 20 MG

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

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

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

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

Waxa ay tahay inaad sameyso:

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

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

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

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

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

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

Waxa ay tahay inaad sameyso:

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

Metformin ER 750 mg

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

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

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

Waxa ay tahay inaad sameyso:

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

Nortriptyline 10mg Kaabsal

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

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

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

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

Waxa ay tahay inaad sameyso:

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

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

PAROEX 0.12%

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

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

Waxa ay tahay inaad sameyso:

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

MESALAMINE 1.2 G

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

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

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

Waxa ay tahay inaad sameyso:

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

NP THYROID 15mg iyo 120mg

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

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

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

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

Waxa ay tahay inaad sameyso:

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

QAADASHADA 5 MCG / HR

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

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

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

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

Waxa ay tahay inaad sameyso:

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

MIBELAS 24 FE 1MG-20 (24)

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

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

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

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

Waxa ay tahay inaad sameyso:

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

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

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

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

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

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

Waxa ay tahay inaad sameyso:

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

Metformin ER 750 mg
(waxaa soo saaray Granules Pharmaceuticals)

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

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

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

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

Waxa ay tahay inaad sameyso:

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

AURYXIA 210MG MIISAANKA

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

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

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

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

Waxa ay tahay inaad sameyso:

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

LISINOPRIL 10 MG

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

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

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

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

Waxa ay tahay inaad sameyso:

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

Metformin ER 500mg iyo 750mg

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

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

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

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

Waxa ay tahay inaad sameyso:

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

NP Thyroid 30mg, 60mg, 90mg

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

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

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

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

Waxa ay tahay inaad sameyso:

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

Kiniiniyada Mirtazapine 15mg

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

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

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

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

Waxa ay tahay inaad sameyso:

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

Oxycodone / acetaminophen kiniiniyada 10 / 325mg

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

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

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

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

Waxa ay tahay inaad sameyso:

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

Kiniiniyada Mirtazapine 15mg

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

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

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

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

Waxa ay tahay inaad sameyso:

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

LISINOPRIL 30 MG

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

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

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

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

Waxa ay tahay inaad sameyso:

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

Kiniiniyada Levetiracetam 750mg

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

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

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

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

Waxa ay tahay inaad sameyso:

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

GLYCOPYRRATE 1 MG

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

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

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

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

Waxa ay tahay inaad sameyso:

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

Gabapentin 100mg Kaabsal

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

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

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

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

Waxa ay tahay inaad sameyso:

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

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

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

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

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

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

Waxa ay tahay inaad sameyso:

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

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

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

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

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

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

Waxa ay tahay inaad sameyso:

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

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

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

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

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

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

Waxa ay tahay inaad sameyso:

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

Sotalol AF 80mg

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

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

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

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

Waxa ay tahay inaad sameyso:

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

Phenytoin 125mg / 5mL ganaax afka ah

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

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

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

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

Waxa ay tahay inaad sameyso:

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

Ranitidine 150mg iyo 300mg Kiniinno

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

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

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

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

Waxa ay tahay inaad sameyso:

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

Lamotrigine 100mg Kiniin

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

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

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

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

Waxa ay tahay inaad sameyso:

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

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

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

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

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

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

Waxa ay tahay inaad sameyso:

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

Nystatin Afka Laga Joojiyo 10,000 oo unug mL

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

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

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

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

Waxa ay tahay inaad sameyso:

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

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

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

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

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

Waxa ay tahay inaad sameyso:

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Dawada la xasuusto: Quetiapine Fumarate 400 mg

Lambarka NDC: 67877024801

Lambarka Naadiga: 7143908

Taariikhda uu dhacayo: November 2020

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

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

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

Dawada la xasuusto: 

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

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

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

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

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

Dawada la xasuusto: Tizanidine HCL 2 mg

Lambarka NDC: 55111017915

Lambarada Lot: T800304

Taariikhda uu dhacayo: 03 / 2021

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

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

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

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

Taariikhda uu dhacayo: 2021 OCT 31, 2021 NOV 30

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

Dawada lagu xasuustoFluticasone 50mcg

Lambarka NDC: 60505-0829-01

Lambarka Naadiga: NJ4501

Taariikhda uu dhacayo: 07 / 2020

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

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

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

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

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

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

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