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

452 recalls · Class I, newest first

Class I · High risk

Lotrimin AF

Chemical Contamination: presence of benzene

Terminated Chemical / undeclared Bayer Healthcare Pharmaceuticals Inc. NDC 11523-0010-2 D-0249-2022
Class I · High risk

Lotrimin Af

Chemical Contamination: presence of benzene

Terminated Chemical / undeclared Bayer Healthcare Pharmaceuticals Inc. NDC 11523-0544-2 D-0248-2022
Class I · High risk

Lotrimin Af

Chemical Contamination: presence of benzene

Terminated Chemical / undeclared Bayer Healthcare Pharmaceuticals Inc. NDC 11523-4140-2 D-0247-2022
Class I · High risk

Lotrimin Af

Chemical Contamination: presence of benzene

Terminated Chemical / undeclared Bayer Healthcare Pharmaceuticals Inc. NDC 11523-1272-2 D-0246-2022
Class I · High risk

365 SKINNY High Intensity Capsules

Marketed Without an Approved NDA/ANDA: FDA analysis found the product to be tainted with undeclared sibutramine, a previously approved drug that was withdrawn from the US market due to safety concerns.

Terminated Chemical / undeclared Je Dois Lavoir LLC D-0631-2022

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