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 15101–15120 of 17,529 recalls

October 2, 2013· Nephron Pharmaceuticals Corp.

Recalled Item: Albuterol Sulfate Inhalation Solution

The Issue: Lack of Assurance of Sterility: Nephron Pharmaceuticals Corporation

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

Class II — Potential Health HazardTerminated
Refund
October 2, 2013· Cardinal Health

Recalled Item: Potassium Chloride

The Issue: Labeling: Incorrect or Missing Package Insert: the package

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

Class III — Low RiskTerminated
Refund
September 30, 2013· G & W Laboratories Inc

Recalled Item: G & W Fluocinolone Acetonide Cream USP 0.025%

The Issue: Failed Content Uniformity Specifications; at the 18 month

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

Class III — Low RiskTerminated
Refund
September 27, 2013· Haute Health, LLC

Recalled Item: Prolifta Dietary Supplement Prolifta

The Issue: Marketed without an Approved NDA/ANDA: Dietary supplement may

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

Class I — Serious Health HazardTerminated
Refund
September 27, 2013· Haute Health, LLC

Recalled Item: Virilis Pro

The Issue: Marketed without an Approved NDA/ANDA: Dietary supplement may

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

Class I — Serious Health HazardTerminated
Refund
September 27, 2013· Haute Health, LLC

Recalled Item: PHUK Sexual Enhancement Ultimate Pleasure

The Issue: Marketed without an Approved NDA/ANDA: Dietary supplement may

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

Class I — Serious Health HazardTerminated
Refund
September 26, 2013· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: LAMOTRIGINE TABLETS

The Issue: CGMP Deviations: Pharmaceuticals were produced and distributed with

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

Class II — Potential Health HazardTerminated
Refund
September 26, 2013· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: CIPROFLOXACIN TABLETS

The Issue: CGMP Deviations: Pharmaceuticals were produced and distributed with

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

Class II — Potential Health HazardTerminated
Refund
September 25, 2013· Sandoz Incorporated

Recalled Item: Hydroxychloroquine Sulfate Tablets

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
September 24, 2013· W.S. Badger Company Inc.

Recalled Item: Badger Kids Broad Spectrum SPF30 Zinc Oxide Sunscreen Lotion Tangerine & Vanilla

The Issue: Microbial Contamination of Non-Sterile Products; Selected lots of

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

Class II — Potential Health HazardTerminated
Refund
September 24, 2013· Hospira Inc.

Recalled Item: Ondansetron Injection

The Issue: Presence of Particular Matter: Potential vendor glass issue

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

Class II — Potential Health HazardTerminated
Refund
September 24, 2013· Hospira Inc.

Recalled Item: Metoclopramide Injection

The Issue: Presence of Particulate Matter: Potential vendor glass issue

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

Class II — Potential Health HazardTerminated
Refund
September 24, 2013· W.S. Badger Company Inc.

Recalled Item: Badger Baby Broad Spectrum SPF 30 Zinc Oxide Sunscreen Lotion

The Issue: Microbial Contamination of Non-Sterile Products; Selected lots of

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

Class II — Potential Health HazardTerminated
Refund
September 23, 2013· Tolmar, Inc.

Recalled Item: Ketoconazole Shampoo

The Issue: Subpotent

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

Class III — Low RiskTerminated
Refund
September 23, 2013· West-Ward Pharmaceutical Corp.

Recalled Item: Irinotecan Hydrochloride Injection

The Issue: Superpotent Drug: a recent review of the USP

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

Class II — Potential Health HazardTerminated
Refund
September 23, 2013· Watson Laboratories Inc

Recalled Item: Next Choice" One Dose Emergency Contraceptive (Levonorgestrel Tablet)

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
September 23, 2013· West-Ward Pharmaceutical Corp.

Recalled Item: Irinotecan Hydrochloride Injection

The Issue: Superpotent Drug: a recent review of the USP

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

Class II — Potential Health HazardTerminated
Refund
September 20, 2013· Valeant Pharmaceuticals North Am

Recalled Item: Acanya (Clindamycin Phosphate and Benzoyl Peroxide) Gel 1.2% and 2.5%

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date:

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

Class III — Low RiskTerminated
Refund
September 19, 2013· Ferring Pharmaceuticals Inc

Recalled Item: ENDOMETRIN (progesterone) Vaginal Insert 100 mg USP

The Issue: Discoloration; due to prolonged heat exposure

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

Class III — Low RiskTerminated
Refund
September 17, 2013· Lupin Pharmaceuticals Inc.

Recalled Item: Quinapril Tablets USP

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund