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 6341–6360 of 17,529 recalls

October 22, 2019· Sanofi-Aventis U.S. LLC

Recalled Item: Regular Strength Zantac 150 mg Distributed by: Chattem

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 HazardOngoing
Refund
October 22, 2019· Green Lumber Holdings, LLC

Recalled Item: Green Lumber Natural Fuel For Men capsule

The Issue: Undeclared Tadalafil

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

Class I — Serious Health HazardTerminated
Refund
October 22, 2019· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Estradiol Vaginal Inserts USP

The Issue: Defective Delivery System: complaints for difficulty in pushing

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

Class II — Potential Health HazardTerminated
Refund
October 22, 2019· Apotex Inc.

Recalled Item: Atorvastatin Calcium Tablets

The Issue: Presence of Foreign Tablets/Capsules: a single tablet of

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

Class III — Low RiskTerminated
Refund
October 21, 2019· Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center

Recalled Item: PF-Succinylcholine Chloride Injection

The Issue: Incorrect labeling: Incorrect or missing lot and/or exp

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

Class III — Low RiskTerminated
Refund
October 18, 2019· Basic Reset Inc.

Recalled Item: Nuovi Firming Masque

The Issue: Marketed without an Approved NDA/ANDA

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

Class II — Potential Health HazardTerminated
Refund
October 18, 2019· Basic Reset Inc.

Recalled Item: Basic Reset CBD Reset 750 True Full Spectrum Wintergreen

The Issue: Marketed without an Approved NDA/ANDA

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

Class II — Potential Health HazardTerminated
Refund
October 18, 2019· Basic Reset Inc.

Recalled Item: Miracle Facelift Masque

The Issue: Marketed without an Approved NDA/ANDA

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

Class II — Potential Health HazardTerminated
Refund
October 18, 2019· Basic Reset Inc.

Recalled Item: Basic Reset CBD Reset 750 True Full Spectrum Cinnamon

The Issue: Marketed without an Approved NDA/ANDA

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

Class II — Potential Health HazardTerminated
Refund
October 18, 2019· Basic Reset Inc.

Recalled Item: Basic Reset Earth Wash Cleaner and Personal Care

The Issue: Marketed without an Approved NDA/ANDA

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

Class II — Potential Health HazardTerminated
Refund
October 18, 2019· Basic Reset Inc.

Recalled Item: Basic Reset Nuovi Skin Toner

The Issue: Marketed without an Approved NDA/ANDA

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

Class II — Potential Health HazardTerminated
Refund
October 18, 2019· Basic Reset Inc.

Recalled Item: Basic Reset CBD Reset 750 True Full Spectrum Natural Flavor

The Issue: Marketed without an Approved NDA/ANDA

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

Class II — Potential Health HazardTerminated
Refund
October 18, 2019· Basic Reset Inc.

Recalled Item: BIOGENYX True Full Spectrum CBD Oil Natural Flavor

The Issue: Marketed without an Approved NDA/ANDA

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

Class II — Potential Health HazardTerminated
Refund
October 18, 2019· Basic Reset Inc.

Recalled Item: BIOGENYX True Full Spectrum CBD Oil Wintergreen

The Issue: Marketed without an Approved NDA/ANDA

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

Class II — Potential Health HazardTerminated
Refund
October 18, 2019· Basic Reset Inc.

Recalled Item: BIOGENYX True Full Spectrum CBD Oil Cinnamon

The Issue: Marketed without an Approved NDA/ANDA

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

Class II — Potential Health HazardTerminated
Refund
October 18, 2019· Basic Reset Inc.

Recalled Item: Basic Reset CBD Reset 2400

The Issue: Marketed without an Approved NDA/ANDA

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

Class II — Potential Health HazardTerminated
Refund
October 18, 2019· Mylan Pharmaceuticals Inc.

Recalled Item: Prasugrel Tablets 5 mg

The Issue: Failed Dissolution Specification: Low out of specification dissolution

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

Class II — Potential Health HazardTerminated
Refund
October 17, 2019· Sandoz Inc

Recalled Item: Neomycin and Polymyxin B Sulfates and Dexamethasone Ophthalmic Suspension

The Issue: Labeling: Incorrect or missing package insert

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

Class III — Low RiskTerminated
Refund
October 17, 2019· Sandoz Inc

Recalled Item: Gatifloxacin Ophthalmic Solution 0.5%

The Issue: Labeling: Incorrect or missing package insert

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

Class III — Low RiskTerminated
Refund
October 17, 2019· AVKARE Inc.

Recalled Item: AVKARE Ranitidine Hydrochloride Capsules 150 mg 500 Capsules Rx Only

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 HazardTerminated
Refund