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 10601–10620 of 17,529 recalls

January 19, 2017· Mylan Pharmaceuticals Inc.

Recalled Item: Mirtazapine Tablets

The Issue: Presence of Foreign Tablets/Capsules; possibility of Glipizide 10

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

Class II — Potential Health HazardTerminated
Refund
January 19, 2017· LEO PHARMA INC

Recalled Item: Calcipotriene Cream 0.0005%

The Issue: Undeclared Excipients

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

Class II — Potential Health HazardTerminated
Refund
January 19, 2017· Mylan Pharmaceuticals Inc.

Recalled Item: glipiZIDE Extended-Release Tablets

The Issue: Presence of Foreign Tablets/Capsules; bottles of Glipizide 5

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

Class II — Potential Health HazardTerminated
Refund
January 18, 2017· VistaPharm, Inc.

Recalled Item: Potassium Chloride Oral Solution

The Issue: Defective Container: Leakage of unit dose cups that

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

Class II — Potential Health HazardTerminated
Refund
January 18, 2017· VistaPharm, Inc.

Recalled Item: Metoclopramide Oral Solution

The Issue: CGMP Deviations: Purified water used to manufacture the

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

Class II — Potential Health HazardTerminated
Refund
January 18, 2017· VistaPharm, Inc.

Recalled Item: Lactulose Solution

The Issue: CGMP Deviations: Purified water used to manufacture the

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

Class II — Potential Health HazardTerminated
Refund
January 18, 2017· VistaPharm, Inc.

Recalled Item: Lactulose Solution

The Issue: CGMP Deviations: Purified water used to manufacture the

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

Class II — Potential Health HazardTerminated
Refund
January 18, 2017· VistaPharm, Inc.

Recalled Item: Nystatin Oral Suspension

The Issue: CGMP Deviations: Purified water used to manufacture the

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

Class II — Potential Health HazardTerminated
Refund
January 18, 2017· VistaPharm, Inc.

Recalled Item: Hydrocodone Bitartrate and Acetaminophen Oral Solution

The Issue: CGMP Deviations: Purified water used to manufacture the

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

Class II — Potential Health HazardTerminated
Refund
January 18, 2017· VistaPharm, Inc.

Recalled Item: Methadone Hydrochloride Oral Concentrate

The Issue: CGMP Deviations: Purified water used to manufacture the

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

Class II — Potential Health HazardTerminated
Refund
January 18, 2017· VistaPharm, Inc.

Recalled Item: Phenytoin Oral Suspension

The Issue: CGMP Deviations: Purified water used to manufacture the

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

Class II — Potential Health HazardTerminated
Refund
January 18, 2017· VistaPharm, Inc.

Recalled Item: Oxycodone Hydrochloride Oral Solution

The Issue: CGMP Deviations: Purified water used to manufacture the

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

Class II — Potential Health HazardTerminated
Refund
January 18, 2017· VistaPharm, Inc.

Recalled Item: Methadone Hydrochloride Oral Concentrate

The Issue: CGMP Deviations: Purified water used to manufacture the

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

Class II — Potential Health HazardTerminated
Refund
January 18, 2017· VistaPharm, Inc.

Recalled Item: Methadone Hydrochloride Oral Concentrate

The Issue: CGMP Deviations: Purified water used to manufacture the

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

Class II — Potential Health HazardTerminated
Refund
January 18, 2017· VistaPharm, Inc.

Recalled Item: Nystatin Oral Suspension

The Issue: CGMP Deviations: Purified water used to manufacture the

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

Class II — Potential Health HazardTerminated
Refund
January 16, 2017· LEO PHARMA INC

Recalled Item: Taclonex (calcipotriene and betamethasone dipropionate) Topical Suspension

The Issue: Labeling: Incorrect or missing package insert: the affected

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

Class III — Low RiskTerminated
Refund
January 16, 2017· Vintage Pharmaceuticals LLC dba Qualitest Pharmaceuticals

Recalled Item: DEXAMETHASONE ELIXIR

The Issue: Failed Impurities/ Degradation Specifications

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

Class III — Low RiskTerminated
Refund
January 13, 2017· AbbVie Inc.

Recalled Item: Duopa (carbidopa and levodopa enteral suspension)

The Issue: Failed Stability Specifications: confirmed out of specification results

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

Class II — Potential Health HazardTerminated
Refund
January 12, 2017· Sun Pharmaceutical Industries, Inc.

Recalled Item: Sun Pharma Carbidopa and Levodopa Tablets USP 25 mg/250 mg

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
January 12, 2017· Actavis Inc

Recalled Item: Albuterol Sulfate Inhalation Solution

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund