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

411 recalls · Class II, newest first

Class II · Moderate risk

Duloxetine Delayed-Release Capsules

CGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity (NDSRI), N-nitroso-duloxetine, above the proposed interim limit.

Terminated Nitrosamine impurity Golden State Medical Supply Inc. NDC 60429-165-30 D-0568-2024
Class II · Moderate risk

Vasopressin Injection

Subpotent product in addition to having out-of-specification results for impurities.

Terminated Wrong potency / content American Regent, Inc. NDC 0517-1030-01 D-0507-2024
Class II · Moderate risk

Rizatriptan Benzoate Tablets USP

CGMP Deviations: N-Nitroso Desmethyl Rizatriptan Impurity results that are above the FDA acceptable limit.

Ongoing Nitrosamine impurity Glenmark Pharmaceuticals Inc., USA NDC 68462-466-99 D-0533-2024
Class II · Moderate risk

Rizatriptan Benzoate Tablets USP

CGMP Deviations: N-Nitroso Desmethyl Rizatriptan Impurity results that are above the FDA acceptable limit.

Ongoing Nitrosamine impurity Glenmark Pharmaceuticals Inc., USA NDC 68462-465-99 D-0532-2024
Class II · Moderate risk

Drug Vial Label: Zilretta¿

Failed Stability Specifications - at 12 months 2-8 degrees C followed by 6 weeks at 25 degrees C.

Ongoing Stability / shelf life Pacira Pharmaceuticals INC NDC 65250-001-01 D-0546-2024
Class II · Moderate risk

TraMADol HCl 50 mg Tablet

Presence of Foreign Tablets: Manufacturer received a report from a Pharmacist who reported finding a tablet of baclofen in a bottle of 1000-count tramadol

Terminated Particulate / foreign matter RemedyRepack Inc. NDC 70518-3824-00 D-0489-2024
Class II · Moderate risk

Cardura XL

Failed Impurities/Degradation Specifications

Completed Impurity / degradation Viatris Inc NDC 0049-2080-10 D-0603-2024
Class II · Moderate risk

Cardura XL

Failed Impurities/Degradation Specifications

Completed Impurity / degradation Viatris Inc NDC 0049-2040-10 D-0602-2024

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