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

1,525 recalls · Class III, newest first

Class III · Low risk

Benzphetamine tablets

Labeling: Label Mix-up: Bottle labeled as Benzonatate 100 mg capsules contained Benzphetamine 50 mg tablets and a bottle labeled as Benzphetamine 50 mg tablets contained Benzonatate 100 mg capsules.

Terminated Labeling / mix-up Calvin Scott & Company, Inc. NDC 10702-0040-50 D-1123-2022
Class III · Low risk

Phytonadione Tablets 5mg

Failed Impurities/Degradation Specifications:Out of specification during the 24 month stability testing of Impurity D.

Terminated Impurity / degradation Bausch Health Companies, Inc. NDC 68682-170-30 D-0244-2021
Class III · Low risk

Mephyton (phytonadione)

Failed Impurities/Degradation Specifications:Out of specification during the 24 month stability testing of Impurity D.

Terminated Impurity / degradation Bausch Health Companies, Inc. NDC 0187-1704-05 D-0243-2021
Class III · Low risk

Benzhydrocodone and Acetaminophen Tablets

Failed Impurities/Degradation Specifications; out of specification results obtained for N-Oxide impurity during the 12-month long term stability testing for Batch# 15892A

Terminated Impurity / degradation KVK-Tech, Inc. NDC 10702-344-01 D-0224-2021
Class III · Low risk

Fentanyl

Subpotency: Out-of-specification stability test result for low potency was obtained.

Terminated Wrong potency / content SCA Pharmaceuticals D-0147-2021
Class III · Low risk

Levocetirizine Dihydrochloride Tablets

Failed Impurities/Degradation Specifications: One lot of Levocetirizine dihydrochloride tablets 5 mg 30 count failed stability testing.

Terminated Impurity / degradation InvaTech Pharma Solutions, LLC NDC 10135-0639-30 D-0115-2021
Class III · Low risk

Testosterone Gel 1%

Superpotent Drug: High out-of-specification assay results were obtained during stability testing.

Terminated Wrong potency / content Teva Pharmaceuticals USA NDC 0591-3216-17 D-0100-2021
Class III · Low risk

Felodipine Extended Release Tablets

Failed impurities/ degradation specifications: Out of specification impurity results were observed during routine testing of stability samples for the impurity Felodipine Related compound A

Terminated Impurity / degradation Heritage Pharmaceuticals Inc NDC 23155-050-01 D-0108-2021
Class III · Low risk

Dextroamphetamine Saccharate

Labeling: Incorrect expiration date. Product dated with 24-month expiration date instead of 18-months.

Terminated Labeling / mix-up ANI Pharmaceuticals, Inc. NDC 43975-282-10 D-0048-2021
Class III · Low risk

Dextroamphetamine Saccharate

Labeling: Incorrect expiration date. Product dated with 24-month expiration date instead of 18-months.

Terminated Labeling / mix-up ANI Pharmaceuticals, Inc. NDC 43975-281-10 D-0047-2021
Class III · Low risk

Dextroamphetamine Saccharate

Labeling: Incorrect expiration date. Product dated with 24-month expiration date instead of 18-months.

Terminated Labeling / mix-up ANI Pharmaceuticals, Inc. NDC 43975-280-10 D-0046-2021
Class III · Low risk

Dextroamphetamine Saccharate

Labeling: Incorrect expiration date. Product dated with 24-month expiration date instead of 18-months.

Terminated Labeling / mix-up ANI Pharmaceuticals, Inc. NDC 43975-279-10 D-0045-2021

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