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 10621–10640 of 17,529 recalls

January 9, 2017· Dr. Reddy's Laboratories, Inc.

Recalled Item: Docetaxel Injection USP

The Issue: Defective Container: Product complaints received of defect in

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

Class II — Potential Health HazardTerminated
Refund
January 7, 2017· Hetero USA Inc

Recalled Item: Montelukast sodium tablets

The Issue: Discoloration: the firm received a complaint of a

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

Class III — Low RiskTerminated
Refund
January 5, 2017· The Harvard Drug Group

Recalled Item: Fluconazole Tablets

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
January 5, 2017· The Harvard Drug Group

Recalled Item: Fluconazole Tablets

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
January 5, 2017· InnovaGel

Recalled Item: Diphenhydramine HCl 25 mg

The Issue: Subpotent

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

Class III — Low RiskTerminated
Refund
January 5, 2017· InnovaGel

Recalled Item: Dye Free Allergy Softgel Gelatin Capsule

The Issue: Subpotent

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

Class III — Low RiskTerminated
Refund
January 5, 2017· Sun Pharmaceutical Industries, Inc.

Recalled Item: Alfuzosin Hydrochloride Extended-release Tablets

The Issue: Presence of Foreign Substance: consumer complaint for foreign

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

Class II — Potential Health HazardTerminated
Refund
January 4, 2017· Mckesson Packaging Services

Recalled Item: Donepezil HCl tablets

The Issue: Supotent: Out of Specification result for assay test

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

Class III — Low RiskTerminated
Refund
December 29, 2016· Hetero Drugs Ltd. - Unit 1

Recalled Item: Finasteride Tablets

The Issue: Failed Tablet/Capsule Specification: Tablets were found to be

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

Class III — Low RiskTerminated
Refund
December 28, 2016· Dr. Reddy's Laboratories, Inc.

Recalled Item: Flucanozole Tablets

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
December 28, 2016· Dr. Reddy's Laboratories, Inc.

Recalled Item: Flucanozole Tablets

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
December 28, 2016· Dr. Reddy's Laboratories, Inc.

Recalled Item: Flucanozole Tablets

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
December 28, 2016· Dr. Reddy's Laboratories, Inc.

Recalled Item: Flucanozole Tablets

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
December 28, 2016· L. Perrigo Company

Recalled Item: Clindamycin Phosphate and Benzoyl Peroxide Gel

The Issue: Microbial Contamination of Non-Sterile Product; small number of

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

Class II — Potential Health HazardTerminated
Refund
December 27, 2016· The Harvard Drug Group

Recalled Item: Aripiprazole Tablets

The Issue: Superpotent Drug; out of specification results for assay

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

Class III — Low RiskTerminated
Refund
December 22, 2016· Aurobindo Pharma USA Inc

Recalled Item: Venlafaxine Hydrochloride extended release capsules

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
December 22, 2016· Roxane Laboratories, Inc.

Recalled Item: Furosemide Tablets USP

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
December 22, 2016· Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals

Recalled Item: TEMAZEPAM CAPSULES USP

The Issue: Failed Stability Specifications

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

Class III — Low RiskTerminated
Refund
December 22, 2016· Sandoz Incorporated

Recalled Item: Nadolol Tablets

The Issue: Failed dissolution specification: recalled due to an out

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

Class II — Potential Health HazardTerminated
Refund
December 21, 2016· Teva Pharmaceuticals USA

Recalled Item: Amoxicillin for Oral Suspension USP

The Issue: Subpotency: due to a low, out of specification

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

Class II — Potential Health HazardTerminated
Refund