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

5 recalls · Class III, newest first

Class III · Low risk

FUROSEMIDE Tablets USP

CGMP Deviations: The active pharmaceutical ingredient (API) intended for use in furosemide oral solution USP was inadvertently used to manufacture the recalled furosemide tablets USP.

Terminated cGMP deviation Boehringer Ingelheim Roxane Inc NDC 0054-4299-31 D-0012-2016
Class III · Low risk

FUROSEMIDE Tablets USP

CGMP Deviations: The active pharmaceutical ingredient (API) intended for use in furosemide oral solution USP was inadvertently used to manufacture the recalled furosemide tablets USP.

Terminated cGMP deviation Boehringer Ingelheim Roxane Inc NDC 0054-4297-31 D-0011-2016
Class III · Low risk

UN1002 Air

CGMP Deviations: Confirmed customer compliant of odor when turning on a cylinder of medical air.

Terminated cGMP deviation Praxair Inc. D-0783-2016
Class III · Low risk

UN1002 Air

CGMP Deviations: Confirmed customer compliant of odor when turning on a cylinder of medical air.

Terminated cGMP deviation Praxair Inc. D-0782-2016

Recalls by year