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 17521–17529 of 17,529 recalls

February 8, 2011· Physicians Total Care, Inc.

Recalled Item: Plavix 75 mg

The Issue: Chemical Contamination: Uncharacteristic moldy odor due to presence

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

Class III — Low RiskTerminated
Refund
January 19, 2011· VistaPharm, Inc.

Recalled Item: METOCLOPRAMIDE ORAL SOLUTION

The Issue: Labeling: Correct Labeled Product Miscart/Mispack: The shipper label

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

Class III — Low RiskTerminated
Refund
November 10, 2010· Physicians Total Care, Inc

Recalled Item: Morphine Sulfate Extended Release tablet

The Issue: Labeling: Label mix-up; Bottles labeled to contain Morphine

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

Class I — Serious Health HazardTerminated
Refund
November 10, 2010· Physicians Total Care, Inc

Recalled Item: Morphine Sulfate Immediate Release tablet

The Issue: Labeling: Label mix-up; Bottles labeled to contain Morphine

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

Class I — Serious Health HazardTerminated
Refund
October 4, 2010· Physicians Total Care, Inc.

Recalled Item: Procrit (epoetin alfa) injection

The Issue: Presence of Particulate Matter: glass delamination

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

Class II — Potential Health HazardTerminated
Refund
March 1, 2010· K C Pharmaceuticals Inc

Recalled Item: Eye Drops advanced relief (Dextran 70 0.1%

The Issue: Labeling: Label Mix-Up: Incorrect back labeling of the

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

Class II — Potential Health HazardTerminated
Refund
June 14, 2007· Apotex Corp.

Recalled Item: Leflunomide tablets

The Issue: Subpotent (Single Ingredient Drug): Distribution of product that

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

Class II — Potential Health HazardTerminated
Refund
June 14, 2007· Apotex Corp.

Recalled Item: Leflunomide tablets

The Issue: Subpotent (Single Ingredient Drug): Distribution of product that

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

Class II — Potential Health HazardTerminated
Refund
February 24, 2006· Merit Medical Systems, Inc

Recalled Item: Merit Convenience Kits containing Cytosol Ophthalmics Balanced Salt Solution

The Issue: Lack of Assurance of Sterility: Procedure kits contain

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

Class I — Serious Health HazardTerminated
Refund