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 14761–14780 of 17,529 recalls

March 3, 2014· Terra-Medica Inc.

Recalled Item: Pleo Ex DROPS 5X

The Issue: Penicillin Cross Contamination

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

Class II — Potential Health HazardTerminated
Refund
March 3, 2014· Terra-Medica Inc.

Recalled Item: Pleo Not TABLETS 5X

The Issue: Penicillin Cross Contamination

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

Class II — Potential Health HazardTerminated
Refund
March 3, 2014· Terra-Medica Inc.

Recalled Item: Pleo Stolo DROPS 6X

The Issue: Penicillin Cross Contamination

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

Class II — Potential Health HazardTerminated
Refund
March 3, 2014· Terra-Medica Inc.

Recalled Item: Pleo Not DROPS

The Issue: Penicillin Cross Contamination

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

Class II — Potential Health HazardTerminated
Refund
March 3, 2014· Terra-Medica Inc.

Recalled Item: Pleo Nota- Quent DROPS 5X

The Issue: Penicillin Cross Contamination

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

Class II — Potential Health HazardTerminated
Refund
March 3, 2014· Terra-Medica Inc.

Recalled Item: Pleo Ex SUPPOSITORIES 3X

The Issue: Penicillin Cross Contamination

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

Class II — Potential Health HazardTerminated
Refund
March 3, 2014· Terra-Medica Inc.

Recalled Item: Pleo Not PORTABLE SIPS 7X

The Issue: Penicillin Cross Contamination

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

Class II — Potential Health HazardTerminated
Refund
February 26, 2014· New England Home Therapies, Inc

Recalled Item: All sterile drugs compounded between 2/21/14 and 2/24/14.

The Issue: Lack of Assurance of Sterility: All compounded products

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

Class II — Potential Health HazardTerminated
Refund
February 26, 2014· Pfizer Us Pharmaceutical Group

Recalled Item: Advil PM Caplets

The Issue: Subpotent Drug: This lot is being recalled because

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

Class III — Low RiskTerminated
Refund
February 20, 2014· GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline

Recalled Item: Nicorette Lozenge

The Issue: Failed Lozenge Specifications; Lozenges are overly thick, overly

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

Class III — Low RiskTerminated
Refund
February 20, 2014· GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline

Recalled Item: Nicotine polacrilex lozenge

The Issue: Failed Lozenge Specifications; Lozenges are overly thick, overly

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

Class III — Low RiskTerminated
Refund
February 20, 2014· GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline

Recalled Item: Nicotine polacrilex lozenge

The Issue: Failed Lozenge Specifications; Lozenges are overly thick, overly

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

Class III — Low RiskTerminated
Refund
February 20, 2014· GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline

Recalled Item: Nicotine polacrilex lozenge

The Issue: Failed Lozenge Specifications; Lozenges are overly thick, overly

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

Class III — Low RiskTerminated
Refund
February 20, 2014· GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline

Recalled Item: Nicorette Lozenge and NicoDerm CQ

The Issue: Failed Lozenge Specifications; Lozenges are overly thick, overly

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

Class III — Low RiskTerminated
Refund
February 20, 2014· GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline

Recalled Item: Nicotine polacrilex lozenge

The Issue: Failed Lozenge Specifications; Lozenges are overly thick, overly

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

Class III — Low RiskTerminated
Refund
February 20, 2014· GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline

Recalled Item: Nicorette (nicotine polacrilex) Lozenges Mini

The Issue: Failed Lozenge Specifications; Lozenges are overly thick, overly

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

Class III — Low RiskTerminated
Refund
February 20, 2014· GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline

Recalled Item: Nicotine polacrilex lozenge

The Issue: Failed Lozenge Specifications; Lozenges are overly thick, overly

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

Class III — Low RiskTerminated
Refund
February 20, 2014· GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline

Recalled Item: Nicorette (nicotine polacrilex) Lozenges Mini

The Issue: Failed Lozenge Specifications; Lozenges are overly thick, overly

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

Class III — Low RiskTerminated
Refund
February 20, 2014· GlaxoSmithKline Consumer Healthcare; dba-GlaxoSmithKline

Recalled Item: Nicotine polacrilex lozenge

The Issue: Failed Lozenge Specifications; Lozenges are overly thick, overly

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

Class III — Low RiskTerminated
Refund
February 19, 2014· Gilead Sciences, Inc.

Recalled Item: Atripla (efavirenz 600 mg/ emtricitabine 200 mg/ tenofovir disoproxil fumarate

The Issue: Presence of Foreign Substance: Red Silicone Rubber Particulates

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

Class III — Low RiskTerminated
Refund