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 2841–2860 of 17,529 recalls

September 27, 2022· Pfizer Inc.

Recalled Item: Aminophylline Injection

The Issue: Presence of Particulate Matter: A complaint was received

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

Class II — Potential Health HazardTerminated
Refund
September 26, 2022· AuroMedics Pharma LLC

Recalled Item: Acyclovir Sodium Injection

The Issue: Presence of Particulate Matter: Customer complaint for a

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

Class II — Potential Health HazardCompleted
Refund
September 26, 2022· AuroMedics Pharma LLC

Recalled Item: Tranexamic Acid Injection

The Issue: Presence of Particulate Matter: Piece of metal found

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

Class III — Low RiskOngoing
Refund
September 21, 2022· Viatris Inc

Recalled Item: Ampicillin for Injection

The Issue: Presence of Particulate Matter: A complaint was received

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

Class II — Potential Health HazardTerminated
Refund
September 21, 2022· Akorn, Inc.

Recalled Item: Rifampin Capsules

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardOngoing
Refund
September 21, 2022· Akorn, Inc.

Recalled Item: Rifampin Capsules

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardOngoing
Refund
September 20, 2022· QuVa Pharma, Inc.

Recalled Item: oxyTOCIN 30 Units/500 mL (0.06 Units/mL) added to 0.9% Sodium Chloride

The Issue: Incorrect Product Formulation: Oxytocin 30 units was added

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

Class III — Low RiskTerminated
Refund
September 19, 2022· UNICHEM PHARMACEUTICALS USA INC

Recalled Item: Clonidine Hydrochloride Tablets

The Issue: Product mix-up:0.2 mg strength Clonidine Hydrochloride Tablets, USP

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

Class III — Low RiskTerminated
Refund
September 16, 2022· Novartis Pharmaceuticals Corporation

Recalled Item: Neoral soft gelatin capsules (cyclosporine capsules

The Issue: CGMP deviations: Out of specification results obtained during

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

Class II — Potential Health HazardTerminated
Refund
September 16, 2022· ALMIRALL, LLC

Recalled Item: Xolegel (ketoconazole) gel 2%

The Issue: Failed Viscosity specification: Slightly higher OOS results obtained

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

Class III — Low RiskTerminated
Refund
September 15, 2022· CIPLA

Recalled Item: Budesonide Inhalation Suspension 0.25mg/2mL

The Issue: Sterility Concerns

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

Class II — Potential Health HazardTerminated
Refund
September 15, 2022· RemedyRepack Inc.

Recalled Item: Lisinopril 10 mg tablets

The Issue: Foreign Object Contamination

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

Class II — Potential Health HazardTerminated
Refund
September 14, 2022· Salon Technologies International Inc

Recalled Item: Antica Farmacista Hand Sanitizer Ocean Citron (ethyl alcohol

The Issue: Chemical Contamination: product found to contain benzene

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

Class I — Serious Health HazardTerminated
Refund
September 14, 2022· Salon Technologies International Inc

Recalled Item: Sanitizing Hand Spray 80% (alcohol 80% v/v) Packaged in 2 FL OZ (60 mL) bottles

The Issue: GMP Deviations: FDA analysis found product to contain

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

Class II — Potential Health HazardTerminated
Refund
September 14, 2022· Dr. Reddy's Laboratories, Inc.

Recalled Item: Phytonadione Injectable Emulsion USP

The Issue: Failed Stability Specifications: Out of specification results reported

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

Class III — Low RiskCompleted
Refund
September 13, 2022· Lupin Pharmaceuticals Inc.

Recalled Item: Lisinopril Tablets USP

The Issue: Foreign Object Contamination

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

Class II — Potential Health HazardTerminated
Refund
September 12, 2022· Direct Rx

Recalled Item: Triamcinolone Acetonide cream

The Issue: CGMP Deviations: Product complaints reporting the product to

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

Class II — Potential Health HazardCompleted
Refund
September 9, 2022· Justified Laboratories

Recalled Item: Skincell Mole & Skin Corrector Serum

The Issue: Marketed Without An Approved NDA/ANDA; Unapproved new drug

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

Class II — Potential Health HazardTerminated
Refund
September 9, 2022· Justified Laboratories

Recalled Item: Skincell Mole & Skin Corrector Serum

The Issue: Marketed Without An Approved NDA/ANDA; Unapproved new drug

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

Class II — Potential Health HazardTerminated
Refund
September 1, 2022· SUPERIOR GLOVE WORKS, LTD.

Recalled Item: Synergy Hand Sanitizer

The Issue: CGMP Deviations: FDA analysis found product to contain

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

Class II — Potential Health HazardTerminated
Refund