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
2 this month

Showing 1541–1560 of 17,529 recalls

November 6, 2023· Taro Pharmaceuticals Inc.

Recalled Item: Hydrocortisone 1% and Acetic Acid 2% Otic Solution USP

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
November 1, 2023· Padagis US LLC

Recalled Item: Trospium Chloride Extended-Release Capsules

The Issue: Failed Tablets/Capsules specifications; missing/broken/extra tablets within the

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

Class II — Potential Health HazardOngoing
Refund
November 1, 2023· Apotex Corp.

Recalled Item: Paroxetine Hydrochloride Tablets USP

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardOngoing
Refund
November 1, 2023· Apotex Corp.

Recalled Item: Paroxetine Hydrochloride Tablets USP

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardOngoing
Refund
November 1, 2023· Apotex Corp.

Recalled Item: Paroxetine Hydrochloride Tablets USP

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardOngoing
Refund
November 1, 2023· Apotex Corp.

Recalled Item: Paroxetine Hydrochloride Tablets USP

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardOngoing
Refund
October 31, 2023· Cardinal Health Inc.

Recalled Item: LEADER brand Dry Eye Relief (Polyethylene Glycol 400

The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial

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

Class I — Serious Health HazardOngoing
Refund
October 31, 2023· Cardinal Health Inc.

Recalled Item: LEADER brand Eye Irritation Relief (Polyvinyl alcohol 0.5%

The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial

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

Class I — Serious Health HazardOngoing
Refund
October 31, 2023· Cardinal Health Inc.

Recalled Item: LEADER brand Lubricant Eye Drops (Carboxymethylcellulose Sodium

The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial

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

Class I — Serious Health HazardOngoing
Refund
October 31, 2023· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Polyvinyl Alcohol 1.4% Lubricating Eye Drops

The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial

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

Class I — Serious Health HazardTerminated
Refund
October 31, 2023· Cardinal Health Inc.

Recalled Item: LEADER brand Dry Eye Relief (Carboxymethylcellulose Sodium

The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial

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

Class I — Serious Health HazardOngoing
Refund
October 31, 2023· Cardinal Health Inc.

Recalled Item: LEADER brand Lubricant Eye Drops (Propylene Glycol

The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial

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

Class I — Serious Health HazardOngoing
Refund
October 31, 2023· Cardinal Health Inc.

Recalled Item: LEADER brand Lubricant Eye Drops (Carboxymethylcellulose Sodium

The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial

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

Class I — Serious Health HazardOngoing
Refund
October 31, 2023· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Lubricating Tears Eye Drops (Dextran/Hypromellose)

The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial

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

Class I — Serious Health HazardTerminated
Refund
October 30, 2023· Grato Holdings, Inc.

Recalled Item: V-FORCE Homeopathic

The Issue: Incorrect Product Formulation: product contains Active Ingredient Glandula

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

Class III — Low RiskTerminated
Refund
October 27, 2023· NCS Healthcare of Kentucky Inc

Recalled Item: Lisinopril Tablets USP 20 mg

The Issue: Presence of Foreign Tablets: Potential of stray tablet(s)

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

Class III — Low RiskTerminated
Refund
October 27, 2023· NCS Healthcare of Kentucky Inc

Recalled Item: Buspirone Hydrochloride Tabs USP 10 mg

The Issue: Presence of Foreign Tablets: Potential of stray tablet(s)

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

Class III — Low RiskTerminated
Refund
October 27, 2023· Amneal Pharmaceuticals of New York, LLC

Recalled Item: Extended Phenytoin Sodium Capsules

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
October 26, 2023· VistaPharm LLC

Recalled Item: Mycophenolate Mofetil for Oral Suspension

The Issue: Defective Container: The adaptor does not fit into

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

Class III — Low RiskTerminated
Refund
October 23, 2023· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Phenytoin Oral Suspension

The Issue: Failed Content Uniformity Specifications

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

Class I — Serious Health HazardTerminated
Refund