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
1 this month

Showing 6721–6740 of 17,529 recalls

August 9, 2019· American Health Packaging

Recalled Item: Carbamazepine

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
August 8, 2019· Alkermes Inc

Recalled Item: Vivitrol (naltrexone for extended-release injectable suspension) 380...

The Issue: Labeling: Not Elsewhere Classified. Drug product kit recalled

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

Class II — Potential Health HazardTerminated
Refund
August 7, 2019· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Clotrimazole and Betamethasone Dipropionate Cream USP

The Issue: Temperature Abuse: Complaints received of liquidy texture

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

Class III — Low RiskTerminated
Refund
August 6, 2019· Akorn, Inc.

Recalled Item: Eptifibatide Injection

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
August 6, 2019· Akorn, Inc.

Recalled Item: Eptifibatide Injection

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
August 6, 2019· Akorn, Inc.

Recalled Item: Eptifibatide Injection

The Issue: Short Fill: fill volume was out of specification

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

Class III — Low RiskTerminated
Refund
August 5, 2019· RemedyRepack Inc.

Recalled Item: Lisinopril/HCTZ 20mg/12.5mg Tablet

The Issue: Presence of Foreign Tablets/Capsules: This is a spin-off

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

Class II — Potential Health HazardTerminated
Refund
July 29, 2019· Aurobindo Pharma USA Inc.

Recalled Item: Simvastatin Tablets

The Issue: Labeling; Incorrect or Missing Lot and/or Exp Date;

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

Class III — Low RiskTerminated
Refund
July 29, 2019· Upsher Smith Laboratories, Inc.

Recalled Item: Bexarotene Capsules

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
July 26, 2019· Medtech Products, Inc.

Recalled Item: Clear Eyes Assorted IRC Display

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality

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

Class II — Potential Health HazardTerminated
Refund
July 26, 2019· Medtech Products, Inc.

Recalled Item: Clear Eyes Assorted Sidekick Floor Stand Display

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality

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

Class II — Potential Health HazardTerminated
Refund
July 26, 2019· Medtech Products, Inc.

Recalled Item: Clear Eyes Maximum Itchy Eye Relief Sidekick Floor Stand Display

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality

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

Class II — Potential Health HazardTerminated
Refund
July 26, 2019· Medtech Products, Inc.

Recalled Item: Clear Eyes Redness Relief Handy Pocket Pal Club Pak Display

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality

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

Class II — Potential Health HazardTerminated
Refund
July 26, 2019· Medtech Products, Inc.

Recalled Item: Clear eyes REDNESS RELIEF (Glycerin 0.25%

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality

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

Class II — Potential Health HazardTerminated
Refund
July 26, 2019· Medtech Products, Inc.

Recalled Item: Clear Eyes Redness Relief Club Pack Display

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality

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

Class II — Potential Health HazardTerminated
Refund
July 26, 2019· Medtech Products, Inc.

Recalled Item: Clear Eyes Maximum Redness Relief Club Pack Display

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality

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

Class II — Potential Health HazardTerminated
Refund
July 26, 2019· Medtech Products, Inc.

Recalled Item: Clear Eyes Maximum Itchy Eye Relief Sidekick Floor Stand Display

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality

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

Class II — Potential Health HazardTerminated
Refund
July 26, 2019· Medtech Products, Inc.

Recalled Item: Clear eyes REDNESS RELIEF (Glycerin 0.25%

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality

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

Class II — Potential Health HazardTerminated
Refund
July 26, 2019· Medtech Products, Inc.

Recalled Item: Clear eyes REDNESS RELIEF (Glycerin 0.25%

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality

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

Class II — Potential Health HazardTerminated
Refund
July 26, 2019· Medtech Products, Inc.

Recalled Item: Clear eyes MAXIMUM REDNESS RELIEF (Glycerin 0.5%

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality

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

Class II — Potential Health HazardTerminated
Refund