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

921 recalls · Class II, newest first

Class II · Moderate risk

Tadalafil Tablets

Incorrect Product Formulation: An incorrect grade of Crospovidone was used to manufacture the product.

Terminated cGMP deviation Sun Pharmaceutical Industries INC NDC 16714-077-01 D-0231-2022
Class II · Moderate risk

Tadalafil Tablets

Incorrect Product Formulation: An incorrect grade of Crospovidone was used to manufacture the product.

Terminated cGMP deviation Sun Pharmaceutical Industries INC NDC 16714-075-01 D-0230-2022
Class II · Moderate risk

Pregabalin Capsules

Failed Tablet/Capsule Specifications: Out of Specification results for particle Size Distribution and Bulk Density of the Active Pharmaceutical Ingredient.

Terminated Failed specification Sun Pharmaceutical Industries INC NDC 47335-687-88 D-0361-2022
Class II · Moderate risk

Ezetimibe and Simvastatin Tablets

Failed Excipient Specification; product manufactured using an excipient found to be OOS for conductivity

Terminated Failed specification Golden State Medical Supply Inc. NDC 51407-193-05 D-0228-2022
Class II · Moderate risk

Ezetimibe and Simvastatin Tablets

Failed Excipient Specifications and Presence of Foreign Tablets/Capsules; product manufactured using an excipient found to be OOS for conductivity and some Ezetimibe and Simvastatin Tablets, 10 mg/10 mg were found in the bottle

Terminated Particulate / foreign matter Golden State Medical Supply Inc. D-0227-2022
Class II · Moderate risk

Lidocaine Hydrochloride Topical Solution USP 4%

CGMP Deviations: Lots recalled because they were manufactured at the same facility using the same components as the products that had cracked seals in caps that were found to be superpotent.

Terminated Wrong potency / content Teligent Pharma, Inc. NDC 52565-009-50 D-0281-2022
Class II · Moderate risk

Lidocaine Hydrochloride Topical Solution USP 4%

CGMP Deviations: Lots recalled because they were manufactured at the same facility using the same components as the products that had cracked seals in caps that were found to be superpotent.

Terminated Wrong potency / content Teligent Pharma, Inc. NDC 63739-997-64 D-0279-2022

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