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 1101–1120 of 17,529 recalls

August 5, 2024· Zeco LLC

Recalled Item: HAND-I-SAN

The Issue: CGMP Deviations: sterile water not used for production

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

Class II — Potential Health HazardOngoing
Refund
August 2, 2024· EMPOWER CLINIC SERVICES LLC

Recalled Item: Empower Pharmacy

The Issue: Sterility Concerns

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

Class II — Potential Health HazardTerminated
Refund
August 1, 2024· Baxter Healthcare Corporation

Recalled Item: Heparin (Heparin Sodium in 0.9% Sodium Chloride Injection)

The Issue: Microbial Contamination of Sterile Products; out of limit

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

Class I — Serious Health HazardOngoing
Refund
August 1, 2024· Amneal Pharmaceuticals, LLC

Recalled Item: Methotrexate Tablets

The Issue: Presence of Foreign Tablets: Potential presence of Fludrocortisone

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

Class III — Low RiskCompleted
Refund
July 31, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Indomethacin Extended-Release Capsules

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardOngoing
Refund
July 31, 2024· Granules Pharmaceuticals Inc.

Recalled Item: Gabapentin Tablets

The Issue: Presence of Foreign Tablets; 3 fused tablets of

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

Class II — Potential Health HazardTerminated
Refund
July 26, 2024· Eugia US LLC

Recalled Item: Progesterone Injection

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

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

Class II — Potential Health HazardOngoing
Refund
July 24, 2024· B. Braun Medical Inc

Recalled Item: 0.9% Sodium Chloride Injection USP

The Issue: Presence of Particulate Matter

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

Class I — Serious Health HazardOngoing
Refund
July 23, 2024· FDC Limited

Recalled Item: Ciprofloxacin ophthalmic solution USP

The Issue: Defective container: unable to get the solution out

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

Class II — Potential Health HazardOngoing
Refund
July 22, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Glenmark

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
July 18, 2024· FDC Limited

Recalled Item: Timolol Maleate Ophthalmic Solution USP

The Issue: Defective container; yellow colored spike from cap lodged

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

Class II — Potential Health HazardOngoing
Refund
July 18, 2024· Granules Consumer Health Inc.

Recalled Item: Acetaminophen

The Issue: Label mix-up: Carton incorrectly labeled

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

Class III — Low RiskTerminated
Refund
July 18, 2024· MAIN PRODUCTS INC

Recalled Item: Umary Acido Hialuronico

The Issue: Undeclared Diclofenac

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

Class I — Serious Health HazardOngoing
Refund
July 12, 2024· Supercore Products Group Inc.

Recalled Item: Gold Hard Steel Plus Liquid

The Issue: Undeclared Acetaminophen

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

Class I — Serious Health HazardOngoing
Refund
July 12, 2024· Supercore Products Group Inc.

Recalled Item: Hard Steel Capsules packaged in 1 count blister packs in boxes of 10

The Issue: Undeclared Acetaminophen

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

Class I — Serious Health HazardOngoing
Refund
July 12, 2024· SoloVital

Recalled Item: Umary Acido Hialuronico

The Issue: Undeclared Diclofenac

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

Class I — Serious Health HazardOngoing
Refund
July 11, 2024· Aurobindo Pharma USA Inc

Recalled Item: Healthy Living Acetaminophen

The Issue: Labeling: Missing Label - some bottles are missing

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

Class I — Serious Health HazardOngoing
Refund
July 10, 2024· Endo Pharmaceuticals, Inc.

Recalled Item: Clonazepam Orally Disintegrating Tablets

The Issue: Labeling: Label Error on Declared Strength; Some cartons

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

Class I — Serious Health HazardTerminated
Refund
July 9, 2024· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Nitrofurantoin Capsules

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
July 8, 2024· Hikma Pharmaceuticals USA Inc.

Recalled Item: Acetaminophen Injection

The Issue: Labeling: Label Mix-up: a bag of Dexmedetomidine HCl

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

Class I — Serious Health HazardOngoing
Refund