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

982 recalls · Class II, newest first

Class II · Moderate risk

Cidofovir Dihydrate

CGMP Deviations: Active Pharmaceutical Ingredient (API) manufacturer is on FDA Import Alert.

Terminated cGMP deviation LGM Pharma LLC D-0486-2019

Recalls by year