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
0 this month

Showing 9941–9960 of 17,529 recalls

August 4, 2017· Amgen, Inc.

Recalled Item: Procrit Epoetin Alfa 40

The Issue: Presence of particulate matter: Visible glass flakes identified

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

Class II — Potential Health HazardTerminated
Refund
August 3, 2017· Amneal Pharmaceuticals of New York, LLC

Recalled Item: Lorazepam Oral Concentrate

The Issue: Defective Delivery System: the dropper measurement markings may

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

Class I — Serious Health HazardTerminated
Refund
August 3, 2017· MEDLINE INDUSTRIES INC

Recalled Item: Vitamin A&D Ointment (petroleum 93.5%)

The Issue: Labeling Mixup; the individual A&D ointment foil packets

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

Class II — Potential Health HazardTerminated
Refund
August 3, 2017· KVK-Tech, Inc.

Recalled Item: Phentermine HCL Capsules

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
August 2, 2017· The Harvard Drug Group

Recalled Item: Rugby Diocto Syrup

The Issue: Microbial contamination of Non-sterile Products; presence of yeast

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

Class II — Potential Health HazardTerminated
Refund
August 2, 2017· The Harvard Drug Group

Recalled Item: Rugby Diocto Liquid

The Issue: Microbial contamination of Non-sterile Products; presence of yeast

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

Class II — Potential Health HazardTerminated
Refund
August 2, 2017· The Harvard Drug Group

Recalled Item: Rugby Aller-chlor (Chlorpheniramine Maleate Syrup

The Issue: Microbial contamination of Non-sterile Products; presence of yeast

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

Class II — Potential Health HazardTerminated
Refund
August 2, 2017· The Harvard Drug Group

Recalled Item: Major Senna Syrup Natural Vegetable Laxative

The Issue: Microbial contamination of Non-sterile Products; presence of yeast

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

Class II — Potential Health HazardTerminated
Refund
August 2, 2017· The Harvard Drug Group

Recalled Item: Rugby Senexon Liquid Natural Vegetable Stimulant

The Issue: Microbial contamination of Non-sterile Products; presence of yeast

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

Class II — Potential Health HazardTerminated
Refund
August 2, 2017· Teva Pharmaceuticals USA

Recalled Item: Glipizide Extended-Release Tablets (anti-diabetic agent)

The Issue: Failed Moisture Limits: out of specification test results

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

Class III — Low RiskTerminated
Refund
August 1, 2017· The Ampt Life, LLC

Recalled Item: NATURAL HERBAL COFFEE AMPT

The Issue: Undeclared Sildenafil

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

Class I — Serious Health HazardTerminated
Refund
July 28, 2017· PD-Rx Pharmaceuticals, Inc.

Recalled Item: Famotidine USP 20 mg

The Issue: Failed Tablet/Capsule Specification: out of specification for tablet

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

Class II — Potential Health HazardTerminated
Refund
July 26, 2017· ICU Medical Inc

Recalled Item: 0.9% Sodium Chloride Injection

The Issue: Presence of Particulate Matter; stainless steel

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

Class II — Potential Health HazardTerminated
Refund
July 26, 2017· HOSPIRA INC, LAKE FOREST

Recalled Item: Hydromorphone Hydrochloride Injection

The Issue: Presence of Particulate Matter: Silicone oil

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

Class II — Potential Health HazardTerminated
Refund
July 26, 2017· HOSPIRA INC, LAKE FOREST

Recalled Item: Hydromorphone Hydrochloride Injection

The Issue: Presence of Particulate Matter: Silicone oil

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

Class II — Potential Health HazardTerminated
Refund
July 26, 2017· HOSPIRA INC, LAKE FOREST

Recalled Item: Hydromorphone Hydrochloride Injection

The Issue: Presence of Particulate Matter: Silicone oil

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

Class II — Potential Health HazardTerminated
Refund
July 25, 2017· Teva Pharmaceuticals USA

Recalled Item: Albuterol Sulfate Inhalation Solution

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
July 24, 2017· EZWeightLossTX LLC

Recalled Item: LaBri's Body Health Atomic 60 Capsules Exclusively distributed worldwide by

The Issue: Marketed Without An Approved NDA/ANDA: Tainted Product Marketed

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

Class I — Serious Health HazardTerminated
Refund
July 24, 2017· EZWeightLossTX LLC

Recalled Item: LaBri's Body Health XPLODE 30 capsules Exclusively distribute worldwide by

The Issue: Marketed Without An Approved NDA/ANDA: Tainted Product Marketed

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

Class I — Serious Health HazardTerminated
Refund
July 24, 2017· Teva Pharmaceuticals USA

Recalled Item: Famotidine Tablets USP

The Issue: Failed Tablet/Capsule Specification; out of specification for tablet

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

Class II — Potential Health HazardTerminated
Refund