Independent register of U.S. FDA drug recalls · updated Oct 11, 2026
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FDA Drug Recalls

18,003 recalls, newest first

Class II · Moderate risk

deb stoko

CGMP Deviations: Product was released to market prior to microbiological testing.

Terminated Microbial contamination S.C. Johnson Professional NDC 11084-010-27 D-0220-2019
Class II · Moderate risk

Ortho-Novum 7/7/7

Labeling: Incorrect Instructions; Instructions included for use with the Veridate dispenser contained instructions for the Dialpak dispenser.

Terminated Labeling / mix-up Janssen Pharmaceuticals, Inc. NDC 50458-178-06 D-0218-2019
Class II · Moderate risk

Ortho-Novum 1/35

Labeling: Incorrect Instructions; Instructions included for use with the Veridate dispenser contained instructions for the Dialpak dispenser.

Terminated Labeling / mix-up Janssen Pharmaceuticals, Inc. NDC 50458-176-28 D-0217-2019
Class II · Moderate risk

Catapres .2

Failed Dissolution Specifications: OOS resultsduring routine stability testing

Terminated Dissolution failure Boehringer Ingelheim Pharmaceuticals, Inc. NDC 0597-0007-01 D-0128-2019
Class II · Moderate risk

children's allergy relief

Failed Impurities/Degradation Specifications: unknown impurity higher than the specified limit was detected during routine stability testing.

Terminated Impurity / degradation Taro Pharmaceuticals U.S.A., Inc. D-0278-2019
Class II · Moderate risk

children's allergy

Failed Impurities/Degradation Specifications: unknown impurity higher than the specified limit was detected during routine stability testing.

Terminated Impurity / degradation Taro Pharmaceuticals U.S.A., Inc. NDC 56062-106-08 D-0277-2019
Class II · Moderate risk

Children's 24 Hour Allergy

Failed Impurities/Degradation Specifications: unknown impurity higher than the specified limit was detected during routine stability testing.

Terminated Impurity / degradation Taro Pharmaceuticals U.S.A., Inc. NDC 41250-106-08 D-0276-2019

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