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 17141–17160 of 17,529 recalls

July 25, 2012· Lloyd Inc. of Iowa

Recalled Item: Levothroid (levothyroxine sodium tablets

The Issue: Subpotent; 9-month stability interval

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

Class II — Potential Health HazardTerminated
Refund
July 25, 2012· American Health Packaging

Recalled Item: Topiramate Tablets

The Issue: Labeling: Label Mix-Up: A typographical error in the

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

Class III — Low RiskTerminated
Refund
July 25, 2012· Lloyd Inc. of Iowa

Recalled Item: Thyro-Tab 0.050 mg.

The Issue: Subpotent; 9-month stability interval

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

Class II — Potential Health HazardTerminated
Refund
July 25, 2012· Lloyd Inc. of Iowa

Recalled Item: Thyro-Tab 0.075 mg.

The Issue: Subpotent; 9-month stability interval

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

Class II — Potential Health HazardTerminated
Refund
July 25, 2012· Lloyd Inc. of Iowa

Recalled Item: Levothroid (levothyroxine sodium tablets

The Issue: Subpotent; 9-month stability interval

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

Class II — Potential Health HazardTerminated
Refund
July 24, 2012· Cadence Pharmaceuticals

Recalled Item: OFIRMEV (acetaminophen) injection

The Issue: Presence of Particulate Matter: The firm initiated the

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

Class II — Potential Health HazardTerminated
Refund
July 23, 2012· Custom Medical Specialties, Inc.

Recalled Item: Custom Access Tray

The Issue: Lack of Assurance of Sterility; the firm's medical

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

Class II — Potential Health HazardTerminated
Refund
July 23, 2012· Custom Medical Specialties, Inc.

Recalled Item: CMS-8934 Custom Phlebectomy Tray

The Issue: Lack of Assurance of Sterility; the firm's medical

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

Class II — Potential Health HazardTerminated
Refund
July 23, 2012· Custom Medical Specialties, Inc.

Recalled Item: CMS-2374-R4 Custom US Breast Core Biopsy Tray

The Issue: Lack of Assurance of Sterility; the firm's medical

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

Class II — Potential Health HazardTerminated
Refund
July 23, 2012· American Health Packaging

Recalled Item: Mercaptopurine Tablets

The Issue: Failed USP Dissolution Test Requirements: This sub-recall is

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

Class II — Potential Health HazardTerminated
Refund
July 23, 2012· Stat Rx USA

Recalled Item: Tizanidine (Generic for: Zanaflex)

The Issue: Labeling: Label Mix-Up; Some bottles of Tizanidine 4mg

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

Class III — Low RiskTerminated
Refund
July 19, 2012· Abbott Laboratories

Recalled Item: Synthroid (levothyroxine sodium) Tablets USP

The Issue: Defective Container: A number of Synthroid bottles have

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

Class II — Potential Health HazardTerminated
Refund
July 19, 2012· Abbott Laboratories

Recalled Item: Synthroid (levothyroxine sodium) Tablets USP

The Issue: Defective Container: A number of Synthroid bottles have

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

Class II — Potential Health HazardTerminated
Refund
July 19, 2012· Abbott Laboratories

Recalled Item: Synthroid (levothyroxine sodium) Tablets USP

The Issue: Defective Container: A number of Synthroid bottles have

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

Class II — Potential Health HazardTerminated
Refund
July 18, 2012· Fougera Pharmaceuticals Inc.

Recalled Item: Fougera Ketoconazole Cream 2%

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
July 18, 2012· LNK International, Inc.

Recalled Item: Walgreens ASPIRIN FREE TENSION HEADACHE

The Issue: Undeclared Excipients

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

Class II — Potential Health HazardTerminated
Refund
July 16, 2012· Coral Rock Man, Inc.

Recalled Item: X-ROCK 3 Day Pill For Men

The Issue: Marketed Without an Approved NDA/ANDA: Products tested positive

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

Class I — Serious Health HazardTerminated
Refund
July 16, 2012· Coral Rock Man, Inc.

Recalled Item: Z-ROCK All Natural Male Supplement. 1 capsule blister pack

The Issue: Marketed Without an Approved NDA/ANDA: Products tested positive

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

Class I — Serious Health HazardTerminated
Refund
July 13, 2012· Island Kinetics dba Covalence

Recalled Item: CosMedix Serious Protection

The Issue: Microbial Contamination of Non Sterile Product; mold

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

Class II — Potential Health HazardTerminated
Refund
July 12, 2012· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate) transdermal system patch

The Issue: Miscalibrated and/or Defective Delivery System: Out of Specification

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

Class II — Potential Health HazardTerminated
Refund