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 6201–6220 of 17,529 recalls

November 25, 2019· AuroMedics Pharma LLC

Recalled Item: Vancomycin Hydrochloride for Injection

The Issue: Discoloration: Product complaints of discoloration after reconstitution of

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

Class II — Potential Health HazardTerminated
Refund
November 25, 2019· OraLabs, Incorporated

Recalled Item: Petroleum jelly (White Petrolatum) USP 100%

The Issue: Undeclared Contaminants

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

Class II — Potential Health HazardTerminated
Refund
November 22, 2019· Amneal Pharmaceuticals, Inc.

Recalled Item: Ranitidine Syrup Oral Solution 15 mg/mL 6. fl. oz. (473 mL)

The Issue: CGMP Deviations: Impurity N-nitrosodimethylamine (NDMA) found in API

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

Class II — Potential Health HazardOngoing
Refund
November 22, 2019· Amneal Pharmaceuticals, Inc.

Recalled Item: Ranitidine Tablets

The Issue: CGMP Deviations: Impurity N-nitrosodimethylamine (NDMA) found in API

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

Class II — Potential Health HazardOngoing
Refund
November 22, 2019· Amneal Pharmaceuticals, Inc.

Recalled Item: Ranitidine Tablets

The Issue: CGMP Deviations: Impurity N-nitrosodimethylamine (NDMA) found in API

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

Class II — Potential Health HazardOngoing
Refund
November 22, 2019· Amneal Pharmaceuticals, Inc.

Recalled Item: Ranitidine Tablets

The Issue: CGMP Deviations: Impurity N-nitrosodimethylamine (NDMA) found in API

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

Class II — Potential Health HazardOngoing
Refund
November 22, 2019· Amneal Pharmaceuticals, Inc.

Recalled Item: Ranitidine Tablets

The Issue: CGMP Deviations: Impurity N-nitrosodimethylamine (NDMA) found in API

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

Class II — Potential Health HazardOngoing
Refund
November 21, 2019· Pacira Pharmaceuticals, Inc.

Recalled Item: EXPAREL

The Issue: Sub Potent Drug: Out of Specification (OOS)

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

Class II — Potential Health HazardTerminated
Refund
November 21, 2019· Preferred Pharmaceuticals, Inc

Recalled Item: Ibuprofen Oral Suspension USP

The Issue: Presence of foreign substance: Ibuprofen Oral Suspension USP

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

Class II — Potential Health HazardTerminated
Refund
November 20, 2019· American Health Packaging

Recalled Item: Ranitidine Tablets

The Issue: CGMP Deviations: Potential N-Nitrosodimethylamine (NDMA) amounts above levels

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

Class II — Potential Health HazardTerminated
Refund
November 20, 2019· Idelle Labs

Recalled Item: SURE 48 hr Confidence Unscented invisible solid Anti-Perspirant & Deodorant

The Issue: Undeclared Api

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

Class III — Low RiskTerminated
Refund
November 20, 2019· Idelle Labs

Recalled Item: SURE 48hr Confidence Regular Original Solid Anti-Perspirant & Deodorant Net

The Issue: Undeclared Api

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

Class III — Low RiskTerminated
Refund
November 20, 2019· Idelle Labs

Recalled Item: SURE 48hr Confidence Nourishing Coconut invisible solid Antiperspirant &...

The Issue: Undeclared Api

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

Class III — Low RiskTerminated
Refund
November 20, 2019· Idelle Labs

Recalled Item: SURE 48hr Confidence Unscented Original Solid Anti-Perspirant & Deodorant Net

The Issue: Undeclared Api

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

Class III — Low RiskTerminated
Refund
November 20, 2019· AuroMedics Pharma LLC

Recalled Item: Mirtazapine Tablets

The Issue: Labeling: Label Error on Declared Strength; cases labelled

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

Class I — Serious Health HazardTerminated
Refund
November 20, 2019· AuroMedics Pharma LLC

Recalled Item: Mirtazapine Tablets

The Issue: Labeling: Label Error on Declared Strength; cases labelled

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

Class I — Serious Health HazardTerminated
Refund
November 19, 2019· AuroMedics Pharma LLC

Recalled Item: Gabapentin Capsules

The Issue: Presence of Foreign Tablets/Capsules: One Losartan/HCTZ tablet was

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

Class II — Potential Health HazardTerminated
Refund
November 19, 2019· Baxter Healthcare Corporation

Recalled Item: 0.9% Sodium Chloride Irrigation USP 5000 mL bags

The Issue: Lack of Assurance of Sterility: Product has the

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

Class II — Potential Health HazardTerminated
Refund
November 15, 2019· Rising Pharmaceuticals, Inc.

Recalled Item: Timolol Maleate USP

The Issue: Labeling: Label mix-up: A case of Timolol Maleate

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

Class III — Low RiskTerminated
Refund
November 15, 2019· Rising Pharmaceuticals, Inc.

Recalled Item: Timolol Maleate Sterile Opthalmic Solution

The Issue: Labeling: Label mix-up: A case of Timolol Maleate

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

Class III — Low RiskTerminated
Refund