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 2721–2740 of 17,529 recalls

December 8, 2022· McGuff Compounding Pharmacy Services, Inc.

Recalled Item: Thiamine Hydrochloride 3000 mg/30 mL (100mg/mL)

The Issue: Presence of Particulate Matter: Presence of foreign substances

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

Class II — Potential Health HazardTerminated
Refund
December 7, 2022· Lupin Pharmaceuticals Inc.

Recalled Item: Quinapril Tablets USP

The Issue: CGMP Deviations: Detection of N-Nitroso-quinapril impurity above the

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

Class II — Potential Health HazardTerminated
Refund
December 7, 2022· Lupin Pharmaceuticals Inc.

Recalled Item: Quinapril Tablets USP

The Issue: CGMP Deviations: Detection of N-Nitroso-quinapril impurity above the

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

Class II — Potential Health HazardTerminated
Refund
December 6, 2022· Glaxosmithkline Consumer Healthcare Holdings DBA Haleon

Recalled Item: Advil Liqui Gels (minis)

The Issue: Labeling: Illegible Label; the adhesive migrated onto a

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

Class I — Serious Health HazardTerminated
Refund
December 6, 2022· Glaxosmithkline Consumer Healthcare Holdings DBA Haleon

Recalled Item: Advil Liqui Gels

The Issue: Labeling: Illegible Label; the adhesive migrated onto a

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

Class I — Serious Health HazardTerminated
Refund
December 6, 2022· Glaxosmithkline Consumer Healthcare Holdings DBA Haleon

Recalled Item: Advil (ibuprofen) Tablets

The Issue: Labeling: Illegible Label; the adhesive migrated onto a

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

Class I — Serious Health HazardTerminated
Refund
December 6, 2022· Camber Pharmaceuticals, Inc

Recalled Item: Lacosamide Oral Solution

The Issue: Failed Excipient Specifications: out of specification result observed

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

Class III — Low RiskTerminated
Refund
December 5, 2022· RemedyRepack Inc.

Recalled Item: Desmopressin Acetate Tablet

The Issue: Subpotent Drug: repackaged product was recalled by the

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

Class II — Potential Health HazardTerminated
Refund
December 2, 2022· GlaxoSmithKline Consumer Healthcare Holdings LLC

Recalled Item: TUMS Antacid

The Issue: Foreign Object Contamination

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

Class II — Potential Health HazardCompleted
Refund
December 2, 2022· GlaxoSmithKline Consumer Healthcare Holdings LLC

Recalled Item: TUMS Antacid

The Issue: Foreign Object Contamination

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

Class II — Potential Health HazardCompleted
Refund
December 2, 2022· GlaxoSmithKline Consumer Healthcare Holdings LLC

Recalled Item: TUMS Antacid

The Issue: Foreign Object Contamination

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

Class II — Potential Health HazardCompleted
Refund
December 2, 2022· GlaxoSmithKline Consumer Healthcare Holdings LLC

Recalled Item: TUMS Antacid

The Issue: Foreign Object Contamination

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

Class II — Potential Health HazardCompleted
Refund
December 2, 2022· GlaxoSmithKline Consumer Healthcare Holdings LLC

Recalled Item: TUMS Antacid

The Issue: Foreign Object Contamination

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

Class II — Potential Health HazardCompleted
Refund
December 2, 2022· GlaxoSmithKline Consumer Healthcare Holdings LLC

Recalled Item: TUMS Antacid

The Issue: Foreign Object Contamination

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

Class II — Potential Health HazardCompleted
Refund
December 2, 2022· GlaxoSmithKline Consumer Healthcare Holdings LLC

Recalled Item: TUMS Antacid

The Issue: Foreign Object Contamination

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

Class II — Potential Health HazardCompleted
Refund
December 1, 2022· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Oxcarbazepine Tablets 600mg

The Issue: Presence of foreign substance

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

Class II — Potential Health HazardTerminated
Refund
December 1, 2022· BayCare Integrated Service Center, LLC /dba BayCare Central Pharmacy

Recalled Item: Iohexol (300 mg Iodine/mL)

The Issue: Mislabeling

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

Class I — Serious Health HazardTerminated
Refund
November 29, 2022· Accord Healthcare, Inc.

Recalled Item: Daptomycin for Injection 350 mg/vial 1 Single-dose vial

The Issue: Labeling mixup: cartons labeled as Daptomycin 350 mg/vial

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

Class I — Serious Health HazardTerminated
Refund
November 29, 2022· OurPharma LLC

Recalled Item: FentaNYL Citrate 2.5 mg/50 mL (50mcg/ml) Injection Solution

The Issue: Underfilled units

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

Class II — Potential Health HazardTerminated
Refund
November 28, 2022· Exela Pharma Sciences LLC

Recalled Item: 8.4% Sodium Bicarbonate Injection

The Issue: Defective Container: Complaints received of vial breakage and

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

Class I — Serious Health HazardTerminated
Refund