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 1421–1440 of 17,529 recalls

January 3, 2024· Lupin Pharmaceuticals Inc.

Recalled Item: Cefixime for Oral Suspension 100mg/5mL

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
January 2, 2024· Dr. Reddy's Laboratories, Inc.

Recalled Item: Tizanidine Tablets

The Issue: Presence of Foreign tablets/capsules - identified as tizanidine

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

Class II — Potential Health HazardCompleted
Refund
December 29, 2023· Strides Pharma Inc.

Recalled Item: Methoxsalen Capsules

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
December 29, 2023· Ascend Laboratories, LLC

Recalled Item: Ibuprofen and Famotidine Tablets 800mg/26.6mg

The Issue: Presence of Foreign Tablet/Capsule: A stray Rasagiline Mesylate

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

Class II — Potential Health HazardOngoing
Refund
December 29, 2023· Rising Pharma Holding, Inc.

Recalled Item: buPROPion Hydrochloride Extended-Release Tablets

The Issue: Presence of Foreign Tablets/Capsules

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

Class II — Potential Health HazardOngoing
Refund
December 28, 2023· Denver Solutions, LLC DBA Leiters Health

Recalled Item: VANCOmycin HCl PF 1.25g added to 0.9% Sodium Chloride 250 mL IV bag

The Issue: Superpotent Drug: semi-automated IV bag filling system can

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

Class I — Serious Health HazardOngoing
Refund
December 28, 2023· Denver Solutions, LLC DBA Leiters Health

Recalled Item: FentaNYL citrate PF

The Issue: Superpotent Drug: semi-automated IV bag filling system can

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

Class I — Serious Health HazardOngoing
Refund
December 28, 2023· Seaway Pharma Inc.

Recalled Item: Premier Value Tussin Cough DM

The Issue: CGMP Deviations: Firm reported possible microbial contamination in

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

Class II — Potential Health HazardOngoing
Refund
December 28, 2023· Seaway Pharma Inc.

Recalled Item: Quality Choice No Drip Extra Moisturizing Nasal Pump Mist Oxymetazoline

The Issue: CGMP Deviations: Firm reported possible microbial contamination in

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

Class II — Potential Health HazardOngoing
Refund
December 28, 2023· Denver Solutions, LLC DBA Leiters Health

Recalled Item: VANCOmycin HCl PF 1.5g added to 0.9% Sodium Chloride 250 mL IV bag

The Issue: Superpotent Drug: semi-automated IV bag filling system can

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

Class I — Serious Health HazardOngoing
Refund
December 28, 2023· Denver Solutions, LLC DBA Leiters Health

Recalled Item: FentaNYL citrate PF

The Issue: Superpotent Drug: semi-automated IV bag filling system can

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

Class I — Serious Health HazardOngoing
Refund
December 28, 2023· Denver Solutions, LLC DBA Leiters Health

Recalled Item: PHENYLephrine HCl 20 mg per 250 mL 0.9% Sodium Chloride (80 mcg per mL)

The Issue: Superpotent Drug: semi-automated IV bag filling system can

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

Class I — Serious Health HazardOngoing
Refund
December 28, 2023· Denver Solutions, LLC DBA Leiters Health

Recalled Item: PHENYLephrine HCl 40 mg per 250 mL 0.9% Sodium Chloride (160 mcg per mL)

The Issue: Superpotent Drug: semi-automated IV bag filling system can

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

Class I — Serious Health HazardOngoing
Refund
December 28, 2023· Seaway Pharma Inc.

Recalled Item: Nasal Spray Original No Drip Oxymetazoline HCl Nasal Solution

The Issue: CGMP Deviations: Firm reported possible microbial contamination in

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

Class II — Potential Health HazardOngoing
Refund
December 28, 2023· Seaway Pharma Inc.

Recalled Item: Quality Choice No Drip Severe Congestion Nasal Pump Mist

The Issue: CGMP Deviations: Firm reported possible microbial contamination in

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

Class II — Potential Health HazardOngoing
Refund
December 28, 2023· Fresenius Medical Care Holdings, Inc.

Recalled Item: DELFLEX Peritoneal Dialysis Solution in Biofine container 1.5% Dextrose

The Issue: Lack of Sterility Assurance

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

Class II — Potential Health HazardOngoing
Refund
December 26, 2023· Amneal Pharmaceuticals of New York, LLC

Recalled Item: Divalproex Sodium 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
December 26, 2023· Haleon US Holdings LLC

Recalled Item: Robitussin Honey CF Max Nighttime Adult (Acetaminophen 650 mg

The Issue: Microbial Contamination of Non-Sterile Products

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

Class I — Serious Health HazardOngoing
Refund
December 26, 2023· Haleon US Holdings LLC

Recalled Item: Robitussin Honey CF Max Non-Drowsy Adult (Acetaminophen 650mg

The Issue: Microbial Contamination of Non-Sterile Products

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

Class I — Serious Health HazardOngoing
Refund
December 26, 2023· Amerisource Health Services LLC

Recalled Item: Benzonatate Capsules

The Issue: Superpotent drug: Assay results were slightly above specification

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

Class III — Low RiskOngoing
Refund