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

966 recalls · Class II, newest first

Class II · Moderate risk

methylcobalamine 1 mg/mL

Lack of Assurance of Sterility: Firm is recalling all unexpired lots of sterile compounded products after FDA inspection found concerns of lack of sterility assurance.

Terminated Sterility / contamination Abbott's Compounding Pharmacy, Inc. D-0686-2016
Class II · Moderate risk

methylcobalamine 10 mg/mL

Lack of Assurance of Sterility: Firm is recalling all unexpired lots of sterile compounded products after FDA inspection found concerns of lack of sterility assurance.

Terminated Sterility / contamination Abbott's Compounding Pharmacy, Inc. D-0685-2016
Class II · Moderate risk

Insulin

Lack of Assurance of Sterility: Firm is recalling all unexpired lots of sterile compounded products after FDA inspection found concerns of lack of sterility assurance.

Terminated Sterility / contamination Abbott's Compounding Pharmacy, Inc. D-0684-2016
Class II · Moderate risk

hydroxyprogesterone w/ pres

Lack of Assurance of Sterility: Firm is recalling all unexpired lots of sterile compounded products after FDA inspection found concerns of lack of sterility assurance.

Terminated Sterility / contamination Abbott's Compounding Pharmacy, Inc. D-0683-2016
Class II · Moderate risk

hydroxyprogesterone in sesame 250 mg/mL

Lack of Assurance of Sterility: Firm is recalling all unexpired lots of sterile compounded products after FDA inspection found concerns of lack of sterility assurance.

Terminated Sterility / contamination Abbott's Compounding Pharmacy, Inc. D-0682-2016
Class II · Moderate risk

Hydroxycobalamine 30 mg/mL

Lack of Assurance of Sterility: Firm is recalling all unexpired lots of sterile compounded products after FDA inspection found concerns of lack of sterility assurance.

Terminated Sterility / contamination Abbott's Compounding Pharmacy, Inc. D-0681-2016
Class II · Moderate risk

Folic Acid

Lack of Assurance of Sterility: Firm is recalling all unexpired lots of sterile compounded products after FDA inspection found concerns of lack of sterility assurance.

Terminated Sterility / contamination Abbott's Compounding Pharmacy, Inc. D-0680-2016
Class II · Moderate risk

Folic Acid

Lack of Assurance of Sterility: Firm is recalling all unexpired lots of sterile compounded products after FDA inspection found concerns of lack of sterility assurance.

Terminated Sterility / contamination Abbott's Compounding Pharmacy, Inc. D-0679-2016
Class II · Moderate risk

Estradiol cypionate/Test cyprionate

Lack of Assurance of Sterility: Firm is recalling all unexpired lots of sterile compounded products after FDA inspection found concerns of lack of sterility assurance.

Terminated Sterility / contamination Abbott's Compounding Pharmacy, Inc. D-0678-2016
Class II · Moderate risk

calcium elemental

Lack of Assurance of Sterility: Firm is recalling all unexpired lots of sterile compounded products after FDA inspection found concerns of lack of sterility assurance.

Terminated Sterility / contamination Abbott's Compounding Pharmacy, Inc. D-0677-2016
Class II · Moderate risk

Bupivacaine

Lack of Assurance of Sterility: Firm is recalling all unexpired lots of sterile compounded products after FDA inspection found concerns of lack of sterility assurance.

Terminated Sterility / contamination Abbott's Compounding Pharmacy, Inc. D-0676-2016
Class II · Moderate risk

Lyrica (pregabalin)

FAILED TABLET/CAPSULE SPECIFICATIONS: Firm is recalling specific lots of pregabalin capsules due to the potential presence of deformed or damaged capsules.

Terminated Failed specification Pfizer Inc. NDC 0071-1014-68 D-0649-2016
Class II · Moderate risk

Lyrica (pregabalin)

FAILED TABLET/CAPSULE SPECIFICATIONS: Firm is recalling specific lots of pregabalin capsules due to the potential presence of deformed or damaged capsules.

Terminated Failed specification Pfizer Inc. NDC 0071-1013-68 D-0648-2016
Class II · Moderate risk

Guaifenesin DM Cherry liquid

Defective Delivery System: Firm recalled Guaifenesin liquid and Guaifenesin DM liquid due incorrect dose markings on the dosing cups.

Terminated Packaging defect Perrigo Company PLC NDC 49348-828-34 D-0587-2016
Class II · Moderate risk

Guaifenesin Grape liquid 100 mg/5 mL

Defective Delivery System: Firm recalled Guaifenesin liquid and Guaifenesin DM liquid due incorrect dose markings on the dosing cups.

Terminated Packaging defect Perrigo Company PLC NDC 37808-288-26 D-0586-2016

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