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 4641–4660 of 17,529 recalls

June 22, 2021· Ardil Comercial S.R.L.

Recalled Item: Limar Hand Sanitizer

The Issue: Labeling Not Elsewhere Classified: Hand sanitizer packaged in

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

Class I — Serious Health HazardOngoing
Refund
June 21, 2021· Prairie Wolf Spirits

Recalled Item: Prairie Wolf Distillery Alcohol Antiseptic 80%

The Issue: Hand sanitizer packaged in bottles that resemble beverage

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

Class I — Serious Health HazardTerminated
Refund
June 18, 2021· Grato Holdings, Inc.

Recalled Item: B-Force

The Issue: Superpotent

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

Class III — Low RiskTerminated
Refund
June 18, 2021· Teva Pharmaceuticals USA

Recalled Item: Topotecan Injection 4 mg/4mL (1 mg/mL)

The Issue: Presence of Particulate Matter: Complaint received of a

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

Class I — Serious Health HazardTerminated
Refund
June 16, 2021· Spirit Pharmaceuticals

Recalled Item: Acetaminophen 325 mg tablets

The Issue: cGMP deviations: Discolored acetaminophen

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

Class II — Potential Health HazardTerminated
Refund
June 10, 2021· CIPLA

Recalled Item: Solifenacin Succinate Tablets

The Issue: CGMP Deviations

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

Class II — Potential Health HazardTerminated
Refund
June 9, 2021· Pfizer Inc.

Recalled Item: Chantix (varenicline) tablets

The Issue: CGMP Deviations: Presence of the N-nitroso-varenicline impurity above

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

Class II — Potential Health HazardOngoing
Refund
June 9, 2021· Pfizer Inc.

Recalled Item: Chantix (varenicline) tablets

The Issue: CGMP Deviations: Presence of the N-nitroso-varenicline impurity above

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

Class II — Potential Health HazardOngoing
Refund
June 9, 2021· Pfizer Inc.

Recalled Item: Chantix (varenicline)Tablets

The Issue: CGMP Deviations: Presence of the N-nitroso-varenicline impurity above

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

Class II — Potential Health HazardOngoing
Refund
June 9, 2021· Genentech Inc

Recalled Item: Xolair (omalizumab) Injection

The Issue: Failed Stability Specifications: Out of Specification results of

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

Class II — Potential Health HazardTerminated
Refund
June 9, 2021· AVKARE Inc.

Recalled Item: Phytonadione Tablets 5 mg

The Issue: Failed Impurities Specification: Out of specification when measuring

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

Class III — Low RiskTerminated
Refund
June 9, 2021· World Source Llc

Recalled Item: QiYu Hand Sanitizer Gel

The Issue: Subpotent

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

Class II — Potential Health HazardTerminated
Refund
June 8, 2021· Bausch Health Companies, Inc.

Recalled Item: Mephyton (Phytonadione) 5 mg tablets

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
June 8, 2021· Bausch Health Companies, Inc.

Recalled Item: Phytonadione Tablets

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
June 8, 2021· Prisma Health Outsourcing Facility

Recalled Item: Ketamine HCl Injection Solution

The Issue: Labeling: Incorrect Exp. Date: Incorrect BUD

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

Class III — Low RiskTerminated
Refund
June 4, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Atorvastatin Calcium Tablets

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
June 1, 2021· VIONA PHARMACEUTICALS INC

Recalled Item: Metformin Hydrochloride Extended-Release Tablets

The Issue: CGMP Deviations: Detection of N-Nitrosodimethylamine (NDMA) levels in

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

Class II — Potential Health HazardTerminated
Refund
May 26, 2021· McKesson Corporation dba McKesson Drug Company

Recalled Item: Levetiracetam Tablets USP

The Issue: Labeling; Wrong Barcode; error in the machine-readable barcode

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

Class III — Low RiskTerminated
Refund
May 21, 2021· Hill Dermaceuticals, Inc.

Recalled Item: DermOtic Oil (fluocinolone acetonide oil) 0.01% Ear Drops 20 mL bottles

The Issue: Presence of Foreign Substance: Potential for broken glass

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

Class II — Potential Health HazardTerminated
Refund
May 20, 2021· Noven Pharmaceuticals Inc

Recalled Item: Daytrana (methylphenidate transdermal system)

The Issue: Defective Delivery System: The number of customer complaints

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

Class II — Potential Health HazardOngoing
Refund