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 15361–15380 of 17,529 recalls

July 22, 2013· Mira Health Products Ltd.

Recalled Item: B-50 capsules

The Issue: Marketed without an Approved NDA/ANDA; product found to

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

Class I — Serious Health HazardTerminated
Refund
July 19, 2013· Bracco Diagnostics Inc

Recalled Item: Tagitol V Barium Sulfate Suspension (40% w/v

The Issue: Failed Stability Specifications: Tagitol V Barium Sulfate Lot

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

Class III — Low RiskTerminated
Refund
July 19, 2013· Watson Laboratories Inc

Recalled Item: Oxycodone and Acetaminophen Capsules

The Issue: Subpotent drug: Two lots of Oxycodone and Acetaminophen

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

Class III — Low RiskTerminated
Refund
July 19, 2013· Herbal Give Care Llc

Recalled Item: Esbelder Fem Mezcla con L-Carnitina Suplemento Alimenticio

The Issue: Undeclared Sibutramine

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

Class I — Serious Health HazardTerminated
Refund
July 19, 2013· Herbal Give Care Llc

Recalled Item: Esbelin Siloutte Mezcal Herbal con L-Carnitine Suplemento Alimenticio

The Issue: Undeclared Sibutramine

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

Class I — Serious Health HazardTerminated
Refund
July 19, 2013· Herbal Give Care Llc

Recalled Item: Esbelder Siloutte Suplemento Alimenticio

The Issue: Undeclared Sibutramine

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

Class I — Serious Health HazardTerminated
Refund
July 19, 2013· Herbal Give Care Llc

Recalled Item: Esbelder Man Herbal Blend With L-Carnitine Dietary Supplement

The Issue: Undeclared Sibutramine

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

Class I — Serious Health HazardTerminated
Refund
July 19, 2013· Myson Corporation, Inc.

Recalled Item: Volcano Male Enhancement Liquid

The Issue: Undeclared Active

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

Class I — Serious Health HazardTerminated
Refund
July 19, 2013· Myson Corporation, Inc.

Recalled Item: Volcano Male Enhancement 1500mg

The Issue: Undeclared Active

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

Class I — Serious Health HazardTerminated
Refund
July 19, 2013· Herbal Give Care Llc

Recalled Item: Esbelin Siloutte Te

The Issue: Undeclared Sibutramine

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

Class I — Serious Health HazardTerminated
Refund
July 18, 2013· Vi-Jon, Inc.

Recalled Item: ALCOHOL FREE ANTISEPTIC (cetylpyridinium chloride) Mouth Rinse

The Issue: Microbial Contamination of Non-Sterile Products: This product is

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

Class III — Low RiskTerminated
Refund
July 18, 2013· GlaxoSmithKline, LLC.

Recalled Item: TUMS

The Issue: Presence of Foreign Tablets/Capsules: Product labeled TUMS Ultra

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

Class III — Low RiskTerminated
Refund
July 17, 2013· Apotex Inc.

Recalled Item: Acyclovir Tablets USP 800 mg

The Issue: Presence of Particulate Matter: Product from lot KF2199,

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

Class II — Potential Health HazardTerminated
Refund
July 15, 2013· Braintree Laboratories Inc.

Recalled Item: Braintree HalfLytely and Bisacodyl Tablet Bowel Prep Kit (Rx) NDC 52268-523-02

The Issue: Defective Container; Small micro fracture observed in the

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

Class III — Low RiskTerminated
Refund
July 12, 2013· Hospira Inc.

Recalled Item: 0.25% Bupivacaine HCl Injection

The Issue: Presence of particulate matter: visible free floating and

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

Class I — Serious Health HazardTerminated
Refund
July 12, 2013· Hospira Inc.

Recalled Item: 0.75% Bupivacaine HCl Injection

The Issue: Presence of particulate matter: visible free floating and

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

Class I — Serious Health HazardTerminated
Refund
July 4, 2013· VistaPharm, Inc.

Recalled Item: Nystatin Oral Suspension

The Issue: Failed Impurites/Degradation Specifications: Test failure of single largest

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

Class II — Potential Health HazardTerminated
Refund
July 3, 2013· Procter & Gamble Co

Recalled Item: DayQuil Sinex DayTime Sinus Relief (acetaminophen 325 mg and phenylephrine

The Issue: Unit Dose Mispackaging: Product packaging defect which could

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

Class II — Potential Health HazardTerminated
Refund
July 2, 2013· Aidapak Services, LLC

Recalled Item: METHYLERGONOVINE MALEATE Tablet

The Issue: Mislabeling

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

Class II — Potential Health HazardTerminated
Refund
July 2, 2013· Aidapak Services, LLC

Recalled Item: NEFAZODONE HCL

The Issue: Mislabeling

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

Class II — Potential Health HazardTerminated
Refund