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 4361–4380 of 17,529 recalls

September 30, 2021· Beiersdorf Inc

Recalled Item: Coppertone Pure & Simple baby 50 Sunscreen Spray (To Deliver) Zinc Oxide 24.08%

The Issue: cGMP Deviations

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

Class II — Potential Health HazardTerminated
Refund
September 30, 2021· Beiersdorf Inc

Recalled Item: Coppertone Pure & Simple 50 Sunscreen Spray (To Deliver) Zinc Oxide 24.08%

The Issue: Chemical contamination; presence of benzene

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

Class I — Serious Health HazardTerminated
Refund
September 28, 2021· Revive Personal Products Company

Recalled Item: The Natural Dentist Healthy Balance Peppermint Sage

The Issue: Labeling; Label mix-up and Wrong Bar Code; back

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

Class II — Potential Health HazardOngoing
Refund
September 28, 2021· Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals

Recalled Item: Butalbital

The Issue: Labeling: Not Elsewhere Classified: the controlled substance classification

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

Class III — Low RiskOngoing
Refund
September 28, 2021· Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals

Recalled Item: Butalbital

The Issue: Labeling: Not Elsewhere Classified: the controlled substance classification

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

Class III — Low RiskOngoing
Refund
September 27, 2021· Strides Pharma Inc.

Recalled Item: Potassium Chloride Extended-Release Tablets

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
September 27, 2021· AMIVAS (US), LLC

Recalled Item: Artesunate for Injection

The Issue: Lack of Assurance of Sterility: Air filter failed

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

Class II — Potential Health HazardTerminated
Refund
September 24, 2021· Eli Lilly & Company

Recalled Item: Glucagon Emergency Kit for Low Blood Sugar

The Issue: SUBPOTENT DRUG: Vial contained a liquid substance, instead

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

Class I — Serious Health HazardTerminated
Refund
September 23, 2021· Monarch PCM, LLC

Recalled Item: Hydroquinone USP

The Issue: Finished product specification did not meet USP specifications

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

Class II — Potential Health HazardTerminated
Refund
September 22, 2021· Teva Pharmaceuticals USA

Recalled Item: AirDuo Digihaler 113/14 (fluticasone propionate 113 mcg and salmeterol 14

The Issue: Subpotent drug: OOS results of Label Claimed Emitted

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

Class II — Potential Health HazardTerminated
Refund
September 22, 2021· Teva Pharmaceuticals USA

Recalled Item: AirDuo Digihaler 55/14 (fluticasone propionate 55 mcg and salmeterol 14

The Issue: Subpotent drug: OOS results of Label Claimed Emitted

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

Class II — Potential Health HazardTerminated
Refund
September 22, 2021· Teva Pharmaceuticals USA

Recalled Item: AirDuo Digihaler 232/14 (fluticasone propionate 232 mcg and salmeterol 14

The Issue: Subpotent drug: OOS results of Label Claimed Emitted

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

Class II — Potential Health HazardTerminated
Refund
September 22, 2021· Teva Pharmaceuticals USA

Recalled Item: AirDuo Digihaler 232/14 (fluticasone propionate 232 mcg and salmeterol 14

The Issue: Subpotent drug: OOS results of Label Claimed Emitted

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

Class II — Potential Health HazardTerminated
Refund
September 22, 2021· Teva Pharmaceuticals USA

Recalled Item: AirDuo Digihaler 113/14 (fluticasone propionate 113 mcg and salmeterol 14

The Issue: Subpotent drug: OOS results of Label Claimed Emitted

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

Class II — Potential Health HazardTerminated
Refund
September 22, 2021· SSM Health Care St. Louis DBA SSM St. Clare Health Center

Recalled Item: Potassium Chloride 40 mEq in 0.9% Sodium Chloride 270 mL NS

The Issue: Sterility Concerns

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

Class II — Potential Health HazardTerminated
Refund
September 22, 2021· New Vitalis Pharmacy LLC dba New Vitalis Pharmacy

Recalled Item: Testosterone Cypionate Testosterone Propionate

The Issue: Sterility Concerns

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

Class II — Potential Health HazardTerminated
Refund
September 21, 2021· Sanitor Corporation

Recalled Item: Cleaning Solutions Foaming Hand Sanitizer

The Issue: CGMP Deviations: Use of this product may cause

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

Class II — Potential Health HazardTerminated
Refund
September 21, 2021· SigmaPharm Laboratories LLC

Recalled Item: Sodium Phenylbutyrate Powder

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
September 17, 2021· American Health Packaging

Recalled Item: GlipiZIDE Extended-Release Tablets

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
September 17, 2021· IntegraDose Compounding Services LLC

Recalled Item: ceFAZolin

The Issue: Lack of sterility assurance

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

Class II — Potential Health HazardTerminated
Refund