Independent register of U.S. FDA drug recalls · updated Oct 11, 2026
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FDA Drug Recalls

14,806 recalls, newest first

Class II · Moderate risk

Testosterone Cypionate Injection

CGMP Deviations: Manufacturing deviations were reported due to an abnormal appearance on parts of machinery.

Terminated cGMP deviation Sun Pharmaceutical Industries INC NDC 62756-015-40 D-1176-2022
Class II · Moderate risk

Testosterone Cypionate Injection

CGMP Deviations: lots made with same active pharmaceutical ingredient (API) as lots that were rejected due to manufacturing issues that could cause the product to be out of specification for impurities.

Terminated Impurity / degradation Sun Pharmaceutical Industries INC NDC 62756-015-40 D-1153-2022
Class II · Moderate risk

Earache Drops

Microbial contamination of non-sterile product.

Terminated Microbial contamination Grato Holdings, Inc. NDC 0363-3233-15 D-0991-2022
Class I · High risk

Tegsedi (inotersen)

Superpotent: High Out of specification (OOS) test result for percent label claim (%LC).

Terminated Wrong potency / content Akcea Therapeutics, Inc. D-1166-2022
Class III · Low risk

Alprostadil Injection USP 500 mcg/mL

Failed Impurities/Degradation Specifications; out-of-specification results for impurities obtained during routine stability testing

Terminated Impurity / degradation Teva Pharmaceuticals USA Inc NDC 0703-1501-02 D-0988-2022

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