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

1,134 recalls, newest first

Class II · Moderate risk

Folinic Acid Mdv Inj

Lack of Assurance of Sterility: The firm is recalling sterile compounded drugs within expiry due to lack of assurance of sterility.

Terminated Sterility / contamination Key Pharmacy and Compounding Center D-0719-2017
Class II · Moderate risk

Folinic Acid Mdv

Lack of Assurance of Sterility: The firm is recalling sterile compounded drugs within expiry due to lack of assurance of sterility.

Terminated Sterility / contamination Key Pharmacy and Compounding Center D-0718-2017
Class II · Moderate risk

Folic Acid 1ml Sdv 10mg/Ml Inj

Lack of Assurance of Sterility: The firm is recalling sterile compounded drugs within expiry due to lack of assurance of sterility.

Terminated Sterility / contamination Key Pharmacy and Compounding Center D-0717-2017
Class II · Moderate risk

Dmso 6.25% Ophth.

Lack of Assurance of Sterility: The firm is recalling sterile compounded drugs within expiry due to lack of assurance of sterility.

Terminated Sterility / contamination Key Pharmacy and Compounding Center D-0715-2017
Class II · Moderate risk

Dmps Acid *5ml* Sdv 50mg/Ml Inj

Lack of Assurance of Sterility: The firm is recalling sterile compounded drugs within expiry due to lack of assurance of sterility.

Terminated Sterility / contamination Key Pharmacy and Compounding Center D-0714-2017
Class II · Moderate risk

Co-Q-10 Oil 20ml Mdv

Lack of Assurance of Sterility: The firm is recalling sterile compounded drugs within expiry due to lack of assurance of sterility.

Terminated Sterility / contamination Key Pharmacy and Compounding Center D-0713-2017
Class II · Moderate risk

Atropine Sulfate 0.5% Ophth

Lack of Assurance of Sterility: The firm is recalling sterile compounded drugs within expiry due to lack of assurance of sterility.

Terminated Sterility / contamination Key Pharmacy and Compounding Center D-0712-2017
Class II · Moderate risk

Atropine Sulfate 0.01% Ophth

Lack of Assurance of Sterility: The firm is recalling sterile compounded drugs within expiry due to lack of assurance of sterility.

Terminated Sterility / contamination Key Pharmacy and Compounding Center D-0711-2017
Class II · Moderate risk

5-Mthf Sdv 5mg/Ml Inj

Lack of Assurance of Sterility: The firm is recalling sterile compounded drugs within expiry due to lack of assurance of sterility.

Terminated Sterility / contamination Key Pharmacy and Compounding Center D-0710-2017
Class II · Moderate risk

5-Mthf 10ml Sdv

Lack of Assurance of Sterility: The firm is recalling sterile compounded drugs within expiry due to lack of assurance of sterility.

Terminated Sterility / contamination Key Pharmacy and Compounding Center D-0709-2017
Class II · Moderate risk

5-Mthf 10ml Mdv

Lack of Assurance of Sterility: The firm is recalling sterile compounded drugs within expiry due to lack of assurance of sterility.

Terminated Sterility / contamination Key Pharmacy and Compounding Center D-0708-2017
Class II · Moderate risk

5-Mthf *10ml* Mdv 5mg/Ml Inj

Lack of Assurance of Sterility: The firm is recalling sterile compounded drugs within expiry due to lack of assurance of sterility.

Terminated Sterility / contamination Key Pharmacy and Compounding Center D-0707-2017
Class II · Moderate risk

Estrone USP

cGMP Deviations; lack of quality assurance.

Terminated cGMP deviation American Pharmaceutical Ingredients LLC D-0919-2017
Class III · Low risk

Zinc Oxide Paste 25%

Labeling: Error on Declared Strength: Error is due to an incorrect value in the Drug Facts Panel. The correct strength is displayed on the primary container.

Terminated Labeling / mix-up Fagron, Inc NDC 51522-0694-5 D-0695-2017
Class II · Moderate risk

Levonorgestrel

CGMP Deviations: these repackaged and redistributed products are being recalled due to a recall notice from the active pharmaceutical ingredient manufacturer for deviations from current Good Manufacturing Practices that were found during a recent FDA inspection.

Terminated cGMP deviation Spectrum Laboratory Products, Inc. D-0882-2017
Class II · Moderate risk

Estradiol (17-B-Estradiol; Estra-1,3,5(10)

CGMP Deviations: these repackaged and redistributed products are being recalled due to a recall notice from the active pharmaceutical ingredient manufacturer for deviations from current Good Manufacturing Practices that were found during a recent FDA inspection.

Terminated cGMP deviation Spectrum Laboratory Products, Inc. D-0881-2017
Class I · High risk

Hyland's Baby Nighttime Teething Tablets

Superpotent Drug: FDA analysis found inconsistent amounts of belladonna alkaloids that may differ from the calculated amount on the product labels.

Terminated Wrong potency / content Standard Homeopathic Company NDC 54973-3197-1 D-0864-2017
Class I · High risk

Hyland's Baby Teething Tablets

Superpotent Drug: FDA analysis found inconsistent amounts of belladonna alkaloids that may differ from the calculated amount on the product labels.

Terminated Wrong potency / content Standard Homeopathic Company NDC 54973-3127-3 D-0863-2017
Class II · Moderate risk

Fentanyl Citrate

Labeling: Not Elsewhere Classified- Diluent used to compound product expired prior to the expiration date assigned to the compounded product.

Terminated Labeling / mix-up PharMedium Services, Llc NDC 61553-605-52 D-1166-2017

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