Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
RxRecalls Get alerts

FDA drug recalls in 2024

Every FDA drug recall initiated in 2024, newest first, with its risk class, status and the reason the FDA recorded. Use the cause and risk filters to narrow the year down.

557 recalls, newest first.

Class II · Moderate risk

Pain Wizard

Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process.

Ongoing Failed specification ARG Laboratories, Inc. D-0520-2024
Class II · Moderate risk

Gordofilm Wart Remover

cGMP Deviations

Completed cGMP deviation Dercher Enterprises, Inc., DBA Gordon Laboratories NDC 10481-3009-01 D-0495-2024
Class III · Low risk

Abilify (aripiprazole)

Cross Contamination with Other Products

Ongoing Cross-contamination Second Tokushima Factory, Otsuka Pharmaceutical Co., Ltd. NDC 59148-011-13 D-0469-2024
Class III · Low risk

Abilify (aripiprazole)

Cross Contamination with Other Products

Ongoing Cross-contamination Second Tokushima Factory, Otsuka Pharmaceutical Co., Ltd. NDC 59148-009-13 D-0468-2024
Class III · Low risk

Abilify (aripiprazole)

Cross Contamination with Other Products

Ongoing Cross-contamination Second Tokushima Factory, Otsuka Pharmaceutical Co., Ltd. NDC 59148-008-13 D-0467-2024
Class III · Low risk

Abilify (aripiprazole)

Cross Contamination with Other Products

Ongoing Cross-contamination Second Tokushima Factory, Otsuka Pharmaceutical Co., Ltd. NDC 59148-007-13 D-0466-2024
Class III · Low risk

Cyclophosphamide for Injection

Labeling: Incorrect or missing Package Insert: There is an error on the Package Insert (PI), section 2.3, Preparation, Handling, and Administration. The concentration of the reconstituted product is listed as '20 mg per vial.' This information should read: '20 mg per mL'.

Terminated Labeling / mix-up X-Gen Pharmaceuticals Inc. NDC 39822-0255-01 D-0434-2024
Class III · Low risk

Cyclophosphamide for Injection

Labeling: Incorrect or missing Package Insert: There is an error on the Package Insert (PI), section 2.3, Preparation, Handling, and Administration. The concentration of the reconstituted product is listed as '20 mg per vial.' This information should read: '20 mg per mL'.

Terminated Labeling / mix-up X-Gen Pharmaceuticals Inc. NDC 39822-0250-01 D-0433-2024
Class II · Moderate risk

Eyesaline

CGMP Deviations

Terminated cGMP deviation Honeywell INC D-0461-2024
Class II · Moderate risk

Isotretinoin Capsules

Superpotent Drug: The 3-month stability result for assay was found to be above specification limit

Ongoing Wrong potency / content Teva Pharmaceuticals USA, Inc NDC 0591-2436-45 D-0439-2024
Class I · High risk

Alcoholada Gel

Chemical Contamination: Product manufactured with ethanol API that contains methanol

Ongoing Chemical / undeclared Aruba Aloe Balm N.V. D-0459-2024

Recalls by year