Independent register of U.S. FDA drug recalls · updated Oct 13, 2026
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FDA Drug Recalls

11,818 recalls · Class II, newest first

Class II · Moderate risk

My Way (levonorgestrel)

Marketed Without an Approved NDA/ANDA: 2-pack configuration did not receive appropriate regulatory approval prior to release.

Terminated Unapproved drug Lupin Pharmaceuticals Inc. D-0838-2018
Class II · Moderate risk

My Way (Levonorgestrel)

Marketed Without an Approved NDA/ANDA: 2-pack configuration did not receive appropriate regulatory approval prior to release.

Terminated Unapproved drug Lupin Pharmaceuticals Inc. D-0837-2018
Class II · Moderate risk

screamin' menthol

CGMP Deviations: Products manufactured with an ingredient that exceed the benzene levels allowed in drug products.

Terminated Chemical / undeclared Ideaz Llc D-0835-2018

Recalls by year