Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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FDA Drug Recalls

1,590 recalls, newest first

Class III · Low risk

Atorvastatin Calcium tablets

Failed Impurities/Degradation Specifications - OOS was observed for ATV Cyclo FP Impurity and Total Degradation Impurities tested at the 18 month stability time point in Atorvastatin Calcium Tablets 40 mg 500 tablets.

Terminated Impurity / degradation Dr. Reddy's Laboratories, Inc. NDC 55111-123-05 D-1079-2018
Class II · Moderate risk

Lidocaine 2.5% and Prilocaine Cream

Failed Impurities/Degredation Specifications: Out of Specification results for an unknown impurity was found during routine stability testing at 12 months.

Terminated Impurity / degradation Akorn, Inc. NDC 50383-667-30 D-1046-2018
Class II · Moderate risk

Valsartan 320 mg tablets

CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.

Terminated Nitrosamine impurity Bryant Ranch Prepack Inc. NDC 71335-0567-2 D-1029-2018
Class II · Moderate risk

Valsartan 320 mg tablets

CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.

Terminated Nitrosamine impurity Bryant Ranch Prepack Inc. NDC 63629-6905-1 D-1028-2018
Class II · Moderate risk

Valsartan 80 mg tablets

CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.

Terminated Nitrosamine impurity Bryant Ranch Prepack Inc. NDC 63629-6922-2 D-1027-2018
Class III · Low risk

Moxifloxacin Ophthalmic Solution USP

Failed Impurities/Degradation Specifications: An out-of-specification result in the related substance test during three month long-term stability study.

Terminated Impurity / degradation Lupin Pharmaceuticals Inc. NDC 68180-422-01 D-1050-2018
Class III · Low risk

Testosterone 200 mg Pellet

Labeling: Incorrect or Missing Lot and/or Exp Date: Incorrect expiration date on label

Terminated Labeling / mix-up Right Value Drug Stores, Inc. D-1047-2018
Class II · Moderate risk

Valsartan tablets 160 mg

Carcinogen impurity detected in API used to manufacture drug product.

Terminated Nitrosamine impurity H J Harkins Company Inc dba Pharma Pac NDC 43547-0369-09 D-1022-2018

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