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 5361–5380 of 17,529 recalls

August 18, 2020· Nanomateriales Sa De Cv

Recalled Item: Zanilast+ Gel Antiseptic Hand Sanitizer (70% Ethyl Alcohol) Packaged in

The Issue: GMP Deviations: Potential to contain 1-propanol

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

Class II — Potential Health HazardTerminated
Refund
August 17, 2020· Maison Terre, LLC

Recalled Item: Goldenseal Root Powder Organic

The Issue: Microbial Contamination of Non-Sterile Products: FDA laboratory analysis

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

Class I — Serious Health HazardTerminated
Refund
August 17, 2020· Mylan Institutional LLC

Recalled Item: Tranexamic Acid Injection

The Issue: Labeling: Label Mix-Up; potential for cartons labeled as

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

Class I — Serious Health HazardTerminated
Refund
August 17, 2020· Mylan Institutional LLC

Recalled Item: Amiodarone Hydrochloride Injection

The Issue: Labeling: Label Mix-Up; potential for cartons labeled as

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

Class I — Serious Health HazardTerminated
Refund
August 14, 2020· Grupo Asimex de Mexico SA de CV

Recalled Item: Florance Morris ANTISEPTIC Hand Sanitizer (ethyl alcohol 70%)

The Issue: Chemical Contamination: FDA analysis found the product contains

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

Class I — Serious Health HazardTerminated
Refund
August 14, 2020· Grupo Asimex de Mexico SA de CV

Recalled Item: Florance Morris ANTISEPTIC Hand Sanitizer (ethyl alcohol 70%)

The Issue: CGMP Deviations: All other lots are being recalled

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

Class II — Potential Health HazardTerminated
Refund
August 14, 2020· Volu-Sol, Inc.

Recalled Item: Volu-Sol Handrub Sanitizing Solution (Ethyl Alcohol

The Issue: Marketed Without an Approved NDA/ANDA: product lists methanol

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

Class I — Serious Health HazardTerminated
Refund
August 14, 2020· SG24 LLC

Recalled Item: SkinGuard 24 All-Day Hand Sanitizer 8 oz. bottle with foam pump

The Issue: Marketed without an Approved NDA/ANDA; product labeled to

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

Class I — Serious Health HazardTerminated
Refund
August 14, 2020· SG24 LLC

Recalled Item: Skin Guard 24 All-Day Hand Sanitizer 1 4"x6" Hand Sanitizing

The Issue: Marketed without an Approved NDA/ANDA; product labeled to

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

Class I — Serious Health HazardTerminated
Refund
August 14, 2020· SG24 LLC

Recalled Item: Skin Guard 24 All-Day Hand Sanitizer 10 mL Pocket Pen Dist by: SG24 LLC

The Issue: Marketed without an Approved NDA/ANDA; product labeled to

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

Class I — Serious Health HazardTerminated
Refund
August 14, 2020· SG24 LLC

Recalled Item: SkinGuard 24 All-Day Hand Sanitizer 2.67 oz. bottle with foam pump

The Issue: Marketed without an Approved NDA/ANDA; product labeled to

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

Class I — Serious Health HazardTerminated
Refund
August 14, 2020· Hikma Pharmaceuticals USA Inc.

Recalled Item: Buprenorphine HCl Injection

The Issue: Sub-potent Drug: Out-of-Specification assay results found at 3

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

Class II — Potential Health HazardTerminated
Refund
August 10, 2020· Par Pharmaceutical Inc.

Recalled Item: BusPIRone Hydrochloride Tablets

The Issue: Failed Impurity /Degradation Specifications

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

Class II — Potential Health HazardTerminated
Refund
August 10, 2020· Aurobindo Pharma USA Inc.

Recalled Item: Sulfamethoxazole and Trimethoprim Tablets

The Issue: Presence of Foreign Substance: product complaints were received

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

Class II — Potential Health HazardTerminated
Refund
August 10, 2020· Sanofi-Aventis U.S. LLC

Recalled Item: Elitek (rasburicase) for injection

The Issue: Failed Stability Specifications: Out of Specification result for

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

Class II — Potential Health HazardOngoing
Refund
August 10, 2020· Lannett Company, Inc.

Recalled Item: Prednisone Tablets

The Issue: Labeling: Label Mix Up: bottle labeled to contain

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

Class II — Potential Health HazardTerminated
Refund
August 7, 2020· Open Book Extracts

Recalled Item: Just Hand Sanitizer (Ethyl Alcohol 73%) Single Use-Packs 100-count NDC

The Issue: Labeling Not Elsewhere Classified: Product labeled to contain

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

Class II — Potential Health HazardTerminated
Refund
August 7, 2020· Open Book Extracts

Recalled Item: Always Be Clean Hand Sanitizer (73% Alcohol) 0.04 FL OZ

The Issue: Labeling Not Elsewhere Classified: Product labeled to contain

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

Class II — Potential Health HazardTerminated
Refund
August 7, 2020· Santa Cruz Biotechnology, Inc

Recalled Item: UltraCruz Hand Sanitizing Gel Antimicrobial (70% Isopropyl Alcohol)

The Issue: Subpotent drug

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

Class II — Potential Health HazardTerminated
Refund
August 6, 2020· Family Pharmacy of Statesville

Recalled Item: Lorazepam 1 mg/mL Infusion Solution in 250 mL bags

The Issue: Sterility Concerns

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

Class II — Potential Health HazardTerminated
Refund