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

1,206 recalls · Class II, newest first

Class II · Moderate risk

Cyclosporine

Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.

Terminated Sterility / contamination Pharmacy Innovations D-0200-2023
Class II · Moderate risk

Cholecalciferol

Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.

Terminated Sterility / contamination Pharmacy Innovations D-0198-2023
Class II · Moderate risk

5-Fluorouracil 1%

Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.

Terminated Sterility / contamination Pharmacy Innovations D-0190-2023
Class II · Moderate risk

Minoxidil 0.75%

Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.

Terminated Sterility / contamination Pharmacy Innovations D-0189-2023
Class II · Moderate risk

Dutasteride 0.1%

Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.

Terminated Sterility / contamination Pharmacy Innovations D-0185-2023
Class II · Moderate risk

Epi-Caine

CGMP Deviations: Raw material recalled by repackager, due to discoloration.

Terminated Failed specification Pine Pharmaceuticals, LLC NDC 69194-0948-1 D-0130-2023
Class II · Moderate risk

Glycopyrrolate Tablets

Failed impurities/degradation specifications: Out of specification for unknown impurities.

Completed Impurity / degradation Avkare LLC NDC 50268-363-15 D-0091-2023
Class II · Moderate risk

Ganciclovir for Injection

Labeling: Label mix-up - one vial was mislabeled as Cladribine Injection 10mg/mL inside a 10-count carton of Ganciclovir 500 mg.

Terminated Labeling / mix-up Hikma Pharmaceuticals USA Inc. NDC 0143-9299-01 D-0090-2023

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