Independent register of U.S. FDA drug recalls · updated Oct 12, 2026
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Class II drug recalls - moderate risk

Class II means the product may cause temporary or medically reversible harm, and serious harm is unlikely. It is by far the largest recall class - most potency, dissolution and labeling problems land here.

14,535 recalls, newest first.

Class II · Moderate risk

Lotrimin AF

cGMP Deviations: manufactured at the same facility where other lots were found to be contaminated with benzene.

Terminated Chemical / undeclared Bayer Healthcare Pharmaceuticals Inc. NDC 11523-4327-1 D-0241-2022
Class II · Moderate risk

Lotrimin Af

cGMP Deviations: manufactured at the same facility where other lots were found to be contaminated with benzene.

Terminated Chemical / undeclared Bayer Healthcare Pharmaceuticals Inc. NDC 11523-0010-2 D-0240-2022
Class II · Moderate risk

Lotrimin Af

cGMP Deviations: manufactured at the same facility where other lots were found to be contaminated with benzene.

Terminated Chemical / undeclared Bayer Healthcare Pharmaceuticals Inc. NDC 11523-0010-1 D-0239-2022
Class II · Moderate risk

Lotrimin Af

cGMP Deviations: manufactured at the same facility where other lots were found to be contaminated with benzene.

Terminated Chemical / undeclared Bayer Healthcare Pharmaceuticals Inc. NDC 11523-0544-2 D-0238-2022
Class II · Moderate risk

Lotrimin Af

cGMP Deviations: manufactured at the same facility where other lots were found to be contaminated with benzene.

Terminated Chemical / undeclared Bayer Healthcare Pharmaceuticals Inc. NDC 11523-4140-2 D-0237-2022
Class II · Moderate risk

Lotrimin Af

cGMP Deviations: manufactured at the same facility where other lots were found to be contaminated with benzene.

Terminated Chemical / undeclared Bayer Healthcare Pharmaceuticals Inc. NDC 11523-1272-2 D-0236-2022
Class II · Moderate risk

The Natural Dentist Healthy Balance Peppermint Sage

Labeling; Label mix-up and Wrong Bar Code; back label incorrectly states active ingredient as Menthol with UPC 7 14132 00071 4 instead of Peppermint Oil and Sage Oil with UPC 7 14132 00073 8

Ongoing Labeling / mix-up Revive Personal Products Company D-0364-2022
Class II · Moderate risk

Artesunate for Injection

Lack of Assurance of Sterility: Air filter failed post integrity test leading to a lack of sterility assurance.

Terminated Sterility / contamination Amivas (US), LLC NDC 73607-001-02 D-0002-2022
Class II · Moderate risk

Hydroquinone USP

Finished product specification did not meet USP specifications.

Terminated Other Monarch PCM, LLC NDC 69367-174-01 D-0855-2021
Class II · Moderate risk

AirDuo Digihaler 55/14

Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol

Terminated Wrong potency / content Teva Pharmaceuticals USA NDC 59310-111-06 D-0023-2022
Class II · Moderate risk

Sodium Phenylbutyrate Powder

Failed Impurities/Degradation Specifications; Out of Specification impurity results obtained during routine testing.

Terminated Impurity / degradation SigmaPharm Laboratories LLC NDC 42794-086-14 D-0898-2021
Class II · Moderate risk

ceFAZolin

Lack of sterility assurance.

Terminated Sterility / contamination IntegraDose Compounding Services LLC NDC 71139-7087-1 D-0896-2021
Class II · Moderate risk

Morphine Sulfate Injection

Defective container: Cracked vials leading to lack of sterility assurance

Terminated Packaging defect Fresenius Kabi USA LLC NDC 63323-452-01 D-0856-2021

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