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

1,586 recalls · Class II, newest first

Class II · Moderate risk

Losartan Potassium Tab. USP 50mg

CGMP Deviations: FDA lab confirmed presence of an impurity, N-Methylnitrosobutyric acid (NMBA) in the finished product above the interim acceptable daily intake level at the manufacturer

Terminated Nitrosamine impurity Preferred Pharmaceuticals, Inc NDC 68788-0048-03 D-1281-2019
Class II · Moderate risk

Ketorolac Tromethamine Injection

Lack of Sterility Assurance: Microbial growth detected during a routine simulation of the manufacturing process, which represents the potential introduction of microorganisms into the products.

Terminated Sterility / contamination Sagent Pharmaceuticals Inc D-1274-2019
Class II · Moderate risk

Losartan Potassium 100 mg

CGMP Deviations: FDA lab confirmed presence of an impurity, N-Methylnitrosobutyric acid (NMBA) in the finished product above the interim acceptable daily intake level per manufacturer

Terminated Nitrosamine impurity Direct Rx NDC 61919-952-30 D-0018-2021
Class II · Moderate risk

Carvedilol Tablets

Labeling; Label Mix-up; report received of one bottle labeled as Acyclovir Tablets USP 400 mg actually contained Carvedilol Tablets 6.25 mg

Terminated Labeling / mix-up Zydus Pharmaceuticals USA Inc NDC 68382-093-05 D-1273-2019
Class II · Moderate risk

Acyclovir Tablets

Labeling; Label Mix-up; report received of one bottle labeled as Acyclovir Tablets USP 400 mg actually contained Carvedilol Tablets 6.25 mg

Terminated Labeling / mix-up Zydus Pharmaceuticals USA Inc NDC 68382-791-01 D-1272-2019
Class II · Moderate risk

Losartan Potassium Tablets

CGMP Deviations: Detection of trace amounts of N-Methylnitrosobutyric acid (NMBA) impurity found in the Active Pharmaceutical Ingredient (API)

Ongoing Nitrosamine impurity Legacy Pharmaceutical Packaging LLC NDC 68645-494-54 D-1263-2019
Class II · Moderate risk

Losartan Potassium Tablets USP 25 mg 50 tablets

CGMP Deviations: FDA lab confirmed presence of an impurity, N-Methylnitrosobutyric acid (NMBA) in the finished product above the interim acceptable daily intake level of 0.96 parts per million.

Ongoing Nitrosamine impurity AVKARE Inc. NDC 50268-516-15 D-1250-2019
Class II · Moderate risk

Losartan Potassium Tablets USP 50 mg 50 tablets

CGMP Deviations: FDA lab confirmed presence of an impurity, N-Methylnitrosobutyric acid (NMBA) in the finished product above the interim acceptable daily intake level of 0.96 parts per million.

Ongoing Nitrosamine impurity AVKARE Inc. NDC 50268-517-15 D-1249-2019
Class II · Moderate risk

Unison Hand Care Products

CGMP Deviations: hand sanitizers and soaps were not produced under current good manufacturing practices.

Terminated cGMP deviation Inopak Ltd D-1319-2019
Class II · Moderate risk

Antibacterial Hand Soap

CGMP Deviations: hand sanitizers and soaps were not produced under current good manufacturing practices.

Terminated cGMP deviation Inopak Ltd D-1318-2019
Class II · Moderate risk

Antibacterial Hand Soap

CGMP Deviations: hand sanitizers and soaps were not produced under current good manufacturing practices.

Terminated cGMP deviation Inopak Ltd D-1315-2019
Class II · Moderate risk

INODERM Antiseptic Hand Soap

CGMP Deviations: hand sanitizers and soaps were not produced under current good manufacturing practices.

Terminated cGMP deviation Inopak Ltd D-1313-2019

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