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

1 recalls · Class II, newest first

Risk Class IClass IIClass III
Status OngoingCompletedTerminated
Year 20262025202420232022 2010 All years
Cause Sterility / contaminationNitrosamine impurityChemical / undeclaredParticulate / foreign matterLabeling / mix-upcGMP deviationMicrobial contamination All causes
Class II · Moderate risk

Eye Drops advanced relief

Labeling: Label Mix-Up: Incorrect back labeling of the immediate container of eye drops (unit carton and front label are correct) which do not list three active ingredients: Dextran 70, PEG 400, and povidone.

Terminated Labeling / mix-up K C Pharmaceuticals Inc D-192-2013

Recalls by year