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 6181–6200 of 17,529 recalls

December 16, 2019· Pharmedium Services, LLC

Recalled Item: NORepinephrine Bitartrate 8 mg added to 250 mL 5% Dextrose

The Issue: Subpotent Drug

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

Class III — Low RiskTerminated
Refund
December 16, 2019· Pharmedium Services, LLC

Recalled Item: NORepinephrine Bitartrate 4 mg added to 250 mL 5% Dextrose

The Issue: Subpotent Drug

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

Class III — Low RiskTerminated
Refund
December 13, 2019· The Harvard Drug Group

Recalled Item: Memantine Hydrochloride Extended-release Capsules

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
December 13, 2019· Granules India Limited

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
December 13, 2019· Lupin Pharmaceuticals Inc.

Recalled Item: Bimatoprost Ophthalmic Solution

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
December 11, 2019· RemedyRepack Inc.

Recalled Item: Ranitidine 150 mg tablet Original Supplier's NDC 65162-0253-10 Remedy Repackaged

The Issue: CGMP Deviation; Received notice from supplier of potential

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

Class II — Potential Health HazardTerminated
Refund
December 11, 2019· Spectrum Laboratory Products

Recalled Item: Estriol [(16a

The Issue: Subpotent Drug: Supplier indicated assay results did not

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

Class II — Potential Health HazardTerminated
Refund
December 10, 2019· Lupin Pharmaceuticals Inc.

Recalled Item: Memantine Hydrochloride Extended-release Capsules

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
December 9, 2019· Asclemed USA Inc. dba Enovachem Pharmaceuticals

Recalled Item: Estriol

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
December 9, 2019· Asclemed USA Inc. dba Enovachem Pharmaceuticals

Recalled Item: Estriol

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
December 9, 2019· Asclemed USA Inc. dba Enovachem Pharmaceuticals

Recalled Item: Estriol

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
December 6, 2019· Lannett Company, Inc.

Recalled Item: Levetiracetam Oral Solution 100mg/mL

The Issue: Microbial Contamination of Non-sterile Products: Out-of-specification results ob

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

Class I — Serious Health HazardTerminated
Refund
December 4, 2019· American Health Packaging

Recalled Item: Raloxifene Hydrochloride 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 2, 2019· AuroMedics Pharma LLC

Recalled Item: Moxifloxacin Ophthalmic Solution USP

The Issue: Discoloration: Market complaints of discoloration in Moxifloxacin Ophthalmic

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

Class III — Low RiskTerminated
Refund
December 2, 2019· Preferred Pharmaceuticals, Inc

Recalled Item: Ranitidine Tablets

The Issue: CGMP Deviations: Presence of NDMA impurity detected in

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

Class II — Potential Health HazardTerminated
Refund
December 2, 2019· Jubilant Cadista Pharmaceuticals, Inc.

Recalled Item: Amantadine Hydrochloride Tablets

The Issue: Foreign Object Contamination

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

Class II — Potential Health HazardTerminated
Refund
November 27, 2019· Pfizer Inc.

Recalled Item: 25% Dextrose Injection

The Issue: Labeling: Incorrect or Missing Lot and/or expiration date

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

Class II — Potential Health HazardTerminated
Refund
November 26, 2019· SCA Pharmaceuticals, LLC

Recalled Item: Lidocaine HCl 2% 5 mL

The Issue: Foreign Object Contamination

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

Class II — Potential Health HazardTerminated
Refund
November 25, 2019· Apothecus Pharmaceutical Corp.

Recalled Item: VCF Vaginal Contraceptive Foam

The Issue: Defective Delivery System: canister unit exhibiting propellant leakage

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

Class III — Low RiskTerminated
Refund
November 25, 2019· Medisca, Inc.

Recalled Item: Estriol

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund