US Drug Recall Register

FDA Drug Recalls

17,898 recalls, newest first

Class II · Moderate risk Terminated

L-Carnitine 27 mL in a 30 mL Vial

Reason Lack of Assurance of Sterility

KRS Global Biotechnology, Inc D-0044-2020
Class II · Moderate risk Terminated

Bimix #3

Reason Lack of Assurance of Sterility

KRS Global Biotechnology, Inc D-0043-2020
Class II · Moderate risk Terminated

Ascorbic Acid

Reason Lack of Assurance of Sterility

KRS Global Biotechnology, Inc D-0041-2020
Class II · Moderate risk Terminated

Ascorbic Acid

Reason Lack of Assurance of Sterility

KRS Global Biotechnology, Inc D-0040-2020
Class II · Moderate risk Terminated

Alpha Lipoic Acid

Reason Lack of Assurance of Sterility

KRS Global Biotechnology, Inc D-0039-2020
Class I · High risk Terminated

Natpara

Reason Defective Delivery System: potential risk of rubber stopper particles clogging the needle and leading to underdosing

Shire Human Genetic Therapies, Inc. D-0038-2020
Class I · High risk Terminated

Natpara

Reason Defective Delivery System: potential risk of rubber stopper particles clogging the needle and leading to underdosing

Shire Human Genetic Therapies, Inc. NDC 68875-0204-02 D-0037-2020
Class I · High risk Terminated

Natpara

Reason Defective Delivery System: potential risk of rubber stopper particles clogging the needle and leading to underdosing

Shire Human Genetic Therapies, Inc. NDC 68875-0203-02 D-0036-2020
Class I · High risk Terminated

Natpara

Reason Defective Delivery System: potential risk of rubber stopper particles clogging the needle and leading to underdosing

Shire Human Genetic Therapies, Inc. NDC 68875-0202-02 D-0035-2020
Class III · Low risk Terminated

Zarontin

Reason Labeling: Incorrect or Missing Lot and/or Exp Date. The expiry date on the product label is incorrect. The label states an expiry date of 09/2021 when it should be 09/2020.

Pfizer Inc. NDC 0071-0237-24 D-0002-2020
Class III · Low risk Terminated

ethosuximide capsules

Reason Labeling: Incorrect or Missing Lot and/or Exp Date. The expiry date on the product label is incorrect. The label states an expiry date of 09/2021 when it should be 09/2020.

Pfizer Inc. NDC 59762-2250-2 D-0001-2020
Class II · Moderate risk Terminated

Oxcarbazepine Oral Suspension

Reason Failed Impurities/Degradation Specificattion

West-Ward Columbus Inc D-1863-2019
Class II · Moderate risk Terminated

Nucala

Reason Temperature Abuse; Product stored and shipped outside of labeled storage requirements.

Cardinal Health dba Specialty Pharmaceutical Services NDC 0173-0892-42 D-1876-2019
Class II · Moderate risk Terminated

Anagrelide Capsules

Reason Failed Impurities/Degradation Specifications: High Out Of Specification results for impurities detected during routine stability testing.

Torrent Pharma Inc. NDC 13668-453-01 D-1862-2019
Class III · Low risk Terminated

Gatifloxacin Ophthalmic Solution 0.5%

Reason Failed Impurities/Degradation Specifications:OOS for unknown impurity.

Mylan Pharmaceuticals Inc. D-1848-2019
Class III · Low risk Terminated

Matzim LA

Reason GMP Deviation: lot not intended for commercial distribution.

Teva Pharmaceuticals USA NDC 52544-692-30 D-0131-2020
Class I · High risk Terminated

Quinacrine Dihydrochloride

Reason Label Mix-Up: Product labeled as Quinacrine Dihydrochloride; however, after testing, identified as Artemisinin.

Darmerica, LLC NDC 71052-530-05 D-0125-2020
Class II · Moderate risk Terminated

Pantoprazole Sodium Delayed Release Tablets

Reason CGMP Deviation: Presence of dark brown discoloration on edges of tablets.

Jubilant Cadista Pharmaceuticals, Inc. NDC 59746-284-90 D-0145-2020