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

1,724 recalls · Class II, newest first

Class II · Moderate risk

Pentreotide

Lack of Processing Controls.

Terminated cGMP deviation Synthetopes Inc D-1399-2019
Class II · Moderate risk

Unison Hand Care Products

CGMP Deviations: hand sanitizers and soaps were not produced under current good manufacturing practices.

Terminated cGMP deviation Inopak Ltd D-1319-2019
Class II · Moderate risk

Antibacterial Hand Soap

CGMP Deviations: hand sanitizers and soaps were not produced under current good manufacturing practices.

Terminated cGMP deviation Inopak Ltd D-1318-2019
Class II · Moderate risk

Antibacterial Hand Soap

CGMP Deviations: hand sanitizers and soaps were not produced under current good manufacturing practices.

Terminated cGMP deviation Inopak Ltd D-1315-2019
Class II · Moderate risk

INODERM Antiseptic Hand Soap

CGMP Deviations: hand sanitizers and soaps were not produced under current good manufacturing practices.

Terminated cGMP deviation Inopak Ltd D-1313-2019
Class II · Moderate risk

Cefdinir for Oral Suspension USP

CGMP Deviations: Product complaints received indicating reconstituted suspension was observed to be thick.

Terminated cGMP deviation Lupin Pharmaceuticals Inc. NDC 68180-723-20 D-0376-2019
Class II · Moderate risk

Cefdinir for Oral Suspension USP

CGMP Deviations: Product complaints received indicating reconstituted suspension was observed to be thick.

Terminated cGMP deviation Lupin Pharmaceuticals Inc. NDC 68180-722-20 D-0375-2019
Class II · Moderate risk

Oxygen

CGMP Deviations

Terminated cGMP deviation Roberts Home Medical LLC D-1002-2019
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

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