Drug Recalls

Here you'll find every drug recall the FDA has issued, including prescription medications, over-the-counter drugs, compounded pharmacy products, and dietary supplements. We've been tracking these since 2006 and our database updates several times a day so you're always looking at current information.

Drugs get recalled for a number of reasons: contamination during manufacturing, incorrect potency or dosage, failed quality testing (like dissolution or stability tests), sterility problems in injectable products, or labeling and packaging errors that could cause someone to take the wrong dose. If you find a product on this list that you use, please follow the instructions provided by the FDA to take the necessary precautions.

17,529 total recalls
2 this month

Showing 1041–1060 of 17,529 recalls

October 9, 2024· Dr. Reddy's Laboratories, Inc.

Recalled Item: Cinacalcet Tablets

The Issue: CGMP Deviations: Presence of N-nitroso Cinacalcet impurity above

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
October 9, 2024· Dr. Reddy's Laboratories, Inc.

Recalled Item: Cinacalcet Tablets

The Issue: CGMP Deviations: Presence of N-nitroso Cinacalcet impurity above

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
October 9, 2024· Dr. Reddy's Laboratories, Inc.

Recalled Item: Cinacalcet Tablets

The Issue: CGMP Deviations: Presence of N-nitroso Cinacalcet impurity above

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
October 8, 2024· Neogen Corporation

Recalled Item: LICEOUT

The Issue: CGMP violations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
October 8, 2024· Neogen Corporation

Recalled Item: LICEOUT

The Issue: CGMP violations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
October 8, 2024· C & A Naturistics

Recalled Item: AK Forte Ortiga y Omega 3 Cont. Neto 100 Tabletas

The Issue: Undeclared Diclofenac

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
October 1, 2024· ACCORD HEALTHCARE, INC.

Recalled Item: Cisplatin Injection

The Issue: Failed Quality Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardTerminated
Refund
September 30, 2024· Staska Pharmaceuticals, Inc.

Recalled Item: Ascorbic Acid Inj. Solution

The Issue: Presence of Particulate Matter: Presence of glass particulates

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardTerminated
Refund
September 30, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Ciclopirox Gel 0.77%

The Issue: Defective Container: Firm received complaints of broken tube

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
September 25, 2024· Fresenius Kabi Compounding, LLC

Recalled Item: Thiamine HCl 0.9% Sodium Chloride Injection USP

The Issue: cGMP violations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardTerminated
Refund
September 25, 2024· Fresenius Kabi Compounding, LLC

Recalled Item: Vancomycin HCl 750 mg per 250 mL 0.9% Sodium Chloride Injection USP

The Issue: cGMP violations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardTerminated
Refund
September 25, 2024· Denison Pharmaceuticals, LLC

Recalled Item: Adult Cough and Chest Congestion (Dextromethorphan HBr USP 20 mg

The Issue: Crystallization: Lack of uniformity - a change in

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
September 25, 2024· Denison Pharmaceuticals, LLC

Recalled Item: Kids' Cough and Chest Congestion (Dextromethorphan HBr

The Issue: Crystallization: Lack of uniformity - a change in

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
September 25, 2024· Fresenius Kabi Compounding, LLC

Recalled Item: NORepinephrine Bitartrate 0.9% Sodium Chloride Injection USP

The Issue: cGMP violations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardTerminated
Refund
September 25, 2024· Fresenius Kabi Compounding, LLC

Recalled Item: NORepinephrine Bitartrate 0.9% Sodium Chloride Injection USP

The Issue: cGMP violations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardTerminated
Refund
September 25, 2024· Fresenius Kabi Compounding, LLC

Recalled Item: Phenylephrine HCl 0.9% Sodium Chloride Injection USP

The Issue: cGMP violations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardTerminated
Refund
September 25, 2024· Fresenius Kabi Compounding, LLC

Recalled Item: EPINEPHrine 0.9% Sodium Chloride Injection USP

The Issue: cGMP violations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardTerminated
Refund
September 25, 2024· Fresenius Kabi Compounding, LLC

Recalled Item: Oxytocin 0.9% Sodium Chloride Injection USP

The Issue: cGMP violations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardTerminated
Refund
September 25, 2024· Fresenius Kabi Compounding, LLC

Recalled Item: Phenylephrine HCl 0.9% Sodium Chloride Injection USP

The Issue: cGMP violations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardTerminated
Refund
September 25, 2024· Fresenius Kabi Compounding, LLC

Recalled Item: Phenylephrine HCl 0.9% Sodium Chloride Injection USP

The Issue: CGMP violations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardTerminated
Refund