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 3901–3920 of 17,529 recalls

January 24, 2022· Ultra Seal Corporation

Recalled Item: Cold Relief Severe Pain/Cough (acetaminophen 325mg

The Issue: cGMP deviations

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

Class II — Potential Health HazardTerminated
Refund
January 24, 2022· Ultra Seal Corporation

Recalled Item: AYPANAL Non-aspirin Pain Reliever (acetaminophen 325 mg) tablets

The Issue: cGMP deviations

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

Class II — Potential Health HazardTerminated
Refund
January 24, 2022· Ultra Seal Corporation

Recalled Item: Regular Strength Pain Reliever (acetaminophen 110 mg

The Issue: cGMP deviations

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

Class II — Potential Health HazardTerminated
Refund
January 24, 2022· Ultra Seal Corporation

Recalled Item: Cold Tablet Pain Reliever/Fever Reducer/Expectorant/Nasal Decongestant...

The Issue: cGMP deviations

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

Class II — Potential Health HazardTerminated
Refund
January 24, 2022· Ultra Seal Corporation

Recalled Item: SINUS DECONGESTANT Nasal Decongestant (phenylephrine HCl 5mg) tablets

The Issue: cGMP deviations

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

Class II — Potential Health HazardTerminated
Refund
January 24, 2022· Ultra Seal Corporation

Recalled Item: REMfresh Advanced Ion-Powered Melatonin (Melatonin 5 mg) Caplets

The Issue: cGMP deviations

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

Class II — Potential Health HazardTerminated
Refund
January 24, 2022· Ultra Seal Corporation

Recalled Item: CETAFEN COUGH & COLD COUGH & COLD RELIEF (Acetaminophen 325 mg

The Issue: cGMP deviations

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

Class II — Potential Health HazardTerminated
Refund
January 24, 2022· Ultra Seal Corporation

Recalled Item: ELECTROLYTE Supplement Tablets (calcium 5.2 mg

The Issue: cGMP deviations

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

Class II — Potential Health HazardTerminated
Refund
January 24, 2022· Ultra Seal Corporation

Recalled Item: Multi-Symptom Cramp Relief (acetaminophen 325mg and Pamabrom 25mg)

The Issue: cGMP deviations

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

Class II — Potential Health HazardTerminated
Refund
January 21, 2022· Mylan Pharmaceuticals Inc

Recalled Item: Proctofoam HC (hydrocortisone acetate 1% and pramoxine hydrochloride 1%) topical

The Issue: cGMP deficiencies

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

Class II — Potential Health HazardTerminated
Refund
January 19, 2022· Dr. Reddy's Laboratories, Inc.

Recalled Item: Azacitidine

The Issue: Failed stability specifications

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

Class III — Low RiskTerminated
Refund
January 19, 2022· Dr. Reddy's Laboratories, Inc.

Recalled Item: Azacitidine

The Issue: Failed stability specifications

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

Class III — Low RiskTerminated
Refund
January 19, 2022· Dr. Reddy's Laboratories, Inc.

Recalled Item: Bortezomib

The Issue: Failed stability specifications

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

Class III — Low RiskTerminated
Refund
January 18, 2022· Teva Pharmaceuticals USA

Recalled Item: Doxylamine Succinate and Pyridoxine Hydrochloride Delayed-Release Tablets 10...

The Issue: Failed Dissolution Specification: Dissolution results are below specification

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

Class II — Potential Health HazardTerminated
Refund
January 14, 2022· Aurobindo Pharma USA Inc.

Recalled Item: Moxifloxacin Ophthalmic Solution

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
January 14, 2022· Mayne Pharma Inc

Recalled Item: Lexette (halobetasol propionate) Topical Foam

The Issue: CGMP Deviation: Difficulty dispensing/does not dispense or dispensing

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

Class II — Potential Health HazardOngoing
Refund
January 12, 2022· Ascend Laboratories, LLC

Recalled Item: Metoprolol Succinate Extended-Release Tablets

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
January 11, 2022· Pharmasol Corporation

Recalled Item: Lung Cleaner (saline eucalyptus) inhaler

The Issue: cGMP deviations

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

Class II — Potential Health HazardTerminated
Refund
January 11, 2022· Exela Pharma Sciences LLC

Recalled Item: 8.4% Sodium Bicarbonate Injection

The Issue: Sterility Concerns

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

Class II — Potential Health HazardTerminated
Refund
January 10, 2022· Teva Pharmaceuticals USA

Recalled Item: Tretinoin Capsules

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund