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
0 this month

Showing 10321–10340 of 17,529 recalls

March 22, 2017· Sun Pharmaceutical Industries, Inc.

Recalled Item: Olanzapine Tablets

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
March 22, 2017· Sun Pharmaceutical Industries, Inc.

Recalled Item: Olanzapine Tablets

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
March 22, 2017· Sun Pharmaceutical Industries, Inc.

Recalled Item: Olanzapine Tablets

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
March 22, 2017· Novartis Pharmaceuticals Corp.

Recalled Item: Isopto Carpine (pilocarpine hydrochloride opthalmic solution) 4%

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
March 22, 2017· Novartis Pharmaceuticals Corp.

Recalled Item: Pilocarpine Hydrochloride Ophthalmic Solution 4%

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
March 22, 2017· GlaxoSmithKline, LLC

Recalled Item: Ventolin HFA (albuterol sulfate) Inhalation Aerosol

The Issue: Defective Delivery System: Elevated number of units with

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

Class II — Potential Health HazardOngoing
Refund
March 21, 2017· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Atorvastatin Calcium Tablets

The Issue: Microbial Contamination of Non-Sterile Products: potential of an

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

Class II — Potential Health HazardTerminated
Refund
March 20, 2017· Valeant Pharmaceuticals North America LLC

Recalled Item: CLENZIderm M.D. Pore Therapy Salicylic Acid 2% Acne Treatment 5 fl. oz. (148 mL)

The Issue: Discoloration

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

Class III — Low RiskTerminated
Refund
March 20, 2017· Valeant Pharmaceuticals North America LLC

Recalled Item: CLENZIderm M.D. Acne Treatment System

The Issue: Discoloration

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

Class III — Low RiskTerminated
Refund
March 20, 2017· G & W Laboratories, Inc.

Recalled Item: Ciclopirox Olamine Cream USP

The Issue: Labeling: Incorrect or Missing Package Insert: product lots

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

Class III — Low RiskTerminated
Refund
March 20, 2017· Mylan Pharmaceuticals Inc.

Recalled Item: Atorvastatin Calcium Tablets

The Issue: Microbial Contamination of Non-Sterile Products: potential of an

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

Class II — Potential Health HazardTerminated
Refund
March 20, 2017· Mylan Pharmaceuticals Inc.

Recalled Item: Atorvastatin Calcium Tablets

The Issue: Microbial Contamination of Non-Sterile Products: potential of an

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

Class II — Potential Health HazardTerminated
Refund
March 20, 2017· Mylan Pharmaceuticals Inc.

Recalled Item: Atorvastatin Calcium Tablets

The Issue: Microbial Contamination of Non-Sterile Products: potential of an

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

Class II — Potential Health HazardTerminated
Refund
March 20, 2017· Mylan Pharmaceuticals Inc.

Recalled Item: Atorvastatin Calcium Tablets

The Issue: Microbial Contamination of Non-Sterile Products: potential of an

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

Class II — Potential Health HazardTerminated
Refund
March 17, 2017· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Fluocinonide Cream UPS

The Issue: Cross contamination with other products: Certain lots of

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

Class III — Low RiskTerminated
Refund
March 17, 2017· Akorn, Inc.

Recalled Item: LATANOPROST OPHTHALMIC SOLUTION

The Issue: Lack of assurance of sterility: product was found

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

Class II — Potential Health HazardTerminated
Refund
March 17, 2017· Shire

Recalled Item: Kalbitor (ecallantide)

The Issue: Presence of Particulate Matter: Glass

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

Class II — Potential Health HazardTerminated
Refund
March 16, 2017· Allergan Sales, LLC

Recalled Item: Lumigan (bimatoprost ophthalmic solution) 0.01%

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
March 16, 2017· Fresenius Kabi USA, LLC

Recalled Item: Fluphenazine Decanoate Injection

The Issue: Subpotent Drug

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

Class III — Low RiskTerminated
Refund
March 15, 2017· Zydus Pharmaceuticals USA Inc

Recalled Item: Divalproex Sodium Delayed 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