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

948 recalls · Class II, newest first

Class II · Moderate risk

PAROXETINE tablets

Failed Impurities/Degradation Specifications-Manufacturer Apotex Inc. recalling lots due to Out of specification results for the excipient Amadori Glucose adduct of Paroxetine

Terminated Impurity / degradation Golden State Medical Supply Inc. NDC 60429-737-30 D-0130-2024
Class II · Moderate risk

PAROXETINE tablets

Failed Impurities/Degradation Specifications-Manufacturer Apotex Inc. recalling lots due to Out of specification results for the excipient Amadori Glucose adduct of Paroxetine

Terminated Impurity / degradation Golden State Medical Supply Inc. NDC 60429-735-90 D-0129-2024
Class II · Moderate risk

PAROXETINE tablets

Failed Impurities/Degradation Specifications-Manufacturer Apotex Inc. recalling lots due to Out of specification results for the excipient Amadori Glucose adduct of Paroxetine

Terminated Impurity / degradation Golden State Medical Supply Inc. NDC 60429-734-30 D-0128-2024

Recalls by year