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Drug Recalls

Drug and Medical Recalls

View the list below of the latest Drug Recall information. The majority of the recalls below originated from either the FDA or the USDA.

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Natural Wellness, Inc. Issues a Nationwide Voluntary Recall of Masxtreme Capsules, Marketed as a Dietary Supplement - 08/24/10

Recall Date: Tuesday, August 24th, 2010

Ikaria® Recalls INOMAX® DS Drug-Delivery System

Recall Date: Tuesday, August 10th, 2010

EZVille, Ltd. Issues a Voluntary Nationwide Recall of Revivexxx® Extra Strength Found to Contain an Undeclared Drug Ingredient

Recall Date: Saturday, August 7th, 2010

Lundbeck Inc. Announces the Voluntary Nationwide Recall of Two Lots of NeoProfen® (ibuprofen lysine) Injection

Recall Date: Saturday, July 31st, 2010

Lundbeck Inc. Announces the Voluntary Nationwide Recall of Two Lots of NeoProfen® (ibuprofen lysine) Injection Recall will Result in Temporary Product Shortage

Recall Date: Friday, July 30th, 2010

Voluntary Recall of PreserVision® Eye Vitamin AREDS 2 Formula in the United States

Recall Date: Tuesday, July 27th, 2010

Bristol-Myers Squibb Initiates a Nationwide Voluntary Recall of Coumadin (R) 1 mg Tablet Blister Packs

Recall Date: Tuesday, July 13th, 2010

McNeil Consumer Healthcare Announces Voluntary Recall of Certain Over-The-Counter (OTC) Products in the United States, Fiji, Guatemala, Dominican Republic, Puerto Rico, Trinidad & Tobago, and Jamaica

Recall Date: Thursday, July 8th, 2010

P&G Voluntarily Recalls 4 Hour Decongestant Nasal Spray in the United States

Recall Date: Friday, June 25th, 2010

Mcneil Consumer Healthcare Recalls Four Product Lots of Benadryl® Allergy Ultratab™ Tablets, 100 Count, and One Product Lot of Extra Strength Tylenol® Rapid Release Gels, 50 Count

Recall Date: Thursday, June 17th, 2010

West-Ward Pharmaceuticals Recalls Ondansetron in 5% Dextrose Injection And Metronidazole Injection, USP Bags Due To Possible Health Risk

Recall Date: Tuesday, June 8th, 2010

Pfizer Initiates a Nationwide Voluntary Recall of All Lots of Metronidazole Injection, Ciprofloxacin Injection, and Ondansetron Injection Bags Made by Claris Lifesciences Due to Non-Sterility

Recall Date: Tuesday, June 8th, 2010

Sagent Pharmaceuticals Initiates a Nationwide Voluntary Recall of All Lots of Ondansetron in 5% Dextrose Injection, 32 mg/50 mL Manufactured by Claris Lifesciences

Recall Date: Monday, June 7th, 2010

Claris Lifesciences initiates a nationwide voluntary recall of all lots of Ciprofloxacin Inj. USP 200 mg / 100 mL, Ciprofloxacin Inj. USP 400 mg / 200 mL, Metronidazole Inj. USP 500 mg/100 ml and Ondansetron Inj., 32 mg / 50 mL.

Recall Date: Wednesday, June 2nd, 2010

Hospira Announces an Expansion of a Nationwide Voluntary Recall of Certain Lots of Liposyn™ and Propofol That May Contain Particulate Matter

Recall Date: Friday, May 28th, 2010

Voluntary Recall of HYLENEX Initiated

Recall Date: Friday, May 21st, 2010

The Medicines Company Expands a Nationwide Recall for Certain Lots of Cleviprex® That May Contain Particulate Matter

Recall Date: Wednesday, March 17th, 2010

McNeil Consumer Healthcare Announces Voluntary Recall of Certain Over-The-Counter (OTC) Products in the Americas, UAE, and Fiji

Recall Date: Friday, January 15th, 2010

Mcneil Consumer Healthcare Announces A Voluntary Nationwide Recall Of All Lots Of Tylenol® Arthritis Pain 100 Count With Ez-Open Cap

Recall Date: Monday, December 28th, 2009

The Medicines Company Issues a Nationwide Recall for Certain Lots of Cleviprex® That May Contain Particulate Matter

Recall Date: Wednesday, December 16th, 2009

Bayer Consumer Care Voluntarily Recalls One Lot of Combination Package of Alka-Seltzer Plus® Day & Night Cold Formula Liquid Gels

Recall Date: Tuesday, December 8th, 2009

P&G Voluntarily Recalls Specific Lots of Vicks Sinex Nasal Spray in the United States, Germany and the United Kingdom

Recall Date: Thursday, November 19th, 2009

RockHard Laboratories Issues a Voluntary Nationwide Recall of Specific Lots of RockHard Weekend marketed as Dietary Supplement

Recall Date: Tuesday, November 17th, 2009

Hospira Issues Nationwide Voluntary Recall of Certain Lots of Liposyn™ and Propofol Products That May Contain Particulate Matter

Recall Date: Monday, November 9th, 2009

American Regent Expands Voluntary Recall to Include All Lots of Ketorolac Tromethamine Injection, USP 15 mg/mL; 1mL Single Dose Vials

Recall Date: Tuesday, November 3rd, 2009

Pointe Scientific, Inc Expands Nationwide Recall of Liquid Glucose Hexokinase Reagent (G7517)

Recall Date: Saturday, October 31st, 2009

Pointe Scientific, Inc Issues Nationwide Recall of Liquid Glucose Hexokinase Reagent (G7517)

Recall Date: Friday, October 30th, 2009

American Regent Voluntarily Recalls All Lots of Ketorolac Tromethamine Injection

Recall Date: Wednesday, October 21st, 2009

FDA Alert: New USP Standards for Heparin Products Will Result in Decreased Potency

Recall Date: Thursday, October 1st, 2009

FDA Warns Consumers Not to Use Stolen Albuterol Sulfate Inhalation Solution and Ipratropium Bromide Inhalation Solution

Recall Date: Thursday, September 17th, 2009

FDA Requires Boxed Warning for Promethazine Hydrochloride Injection

Recall Date: Wednesday, September 16th, 2009

Barr Laboratories, Inc. issues a voluntary nationwide recall of Dextroamphetamine/Amphetamine 20mg Tablets, Lot number 311756

Recall Date: Friday, August 14th, 2009

Young You Corporation Issues a Voluntary Nationwide Recall of Weight Loss Pills Found to Contain an Undeclared Drug Ingredient

Recall Date: Thursday, July 16th, 2009

Teva Pharmaceuticals USA issues a voluntary user-level nationwide recall of Propofol Injectable Emulsion 10 mg/mL 100 mL vials, lot numbers 31305429B and 31305430B

Recall Date: Thursday, July 16th, 2009

Hi-Tech Pharmaceuticals, Inc. Issues Nationwide Recall of All Lots of Stamina-Rx Dietary Supplement Products

Recall Date: Sunday, June 14th, 2009

FoodScience Corporation Recalls Kid's Multivitamin for label Error

Recall Date: Wednesday, June 10th, 2009

AS Medications Solution LLC. Announces a Nationwide Recall of All Lots of Digoxin Tablets 0.25mg Due to Size Variability

Recall Date: Monday, May 11th, 2009

Testosterone Gel Safety Concerns Prompt FDA to Require Label Changes, Medication Guide

Recall Date: Thursday, May 7th, 2009

FDA, FTC Warn Public of Fraudulent 2009 H1N1 Influenza Products

Recall Date: Friday, May 1st, 2009

FDA Requires Boxed Warning for All Botulinum Toxin Products

Recall Date: Thursday, April 30th, 2009

ION Labs Inc. Recalls Influend Cough and Cold Products, in Alabama, Because Of Possible Health Risk

Recall Date: Monday, April 13th, 2009

FDA Obtains Permanent Injunction Barring Two Companies from Manufacturing and Distributing Unapproved Drugs

Recall Date: Friday, April 10th, 2009

Caraco Pharmaceutical Laboratories, Ltd. Announces a Nationwide Voluntary Recall of All Lots of Digoxin Tablets Due to Size Variability

Recall Date: Tuesday, March 31st, 2009

Watson Announces a Nationwide Voluntary Recall of Propafenone HCL Tablets Due to Oversized Tablets

Recall Date: Monday, March 23rd, 2009

FDA Requires Boxed Warning and Risk Mitigation Strategy for Metoclopramide-Containing Drugs

Recall Date: Thursday, February 26th, 2009

ETHEX Corporation Issues Voluntary Nationwide Recall

Recall Date: Tuesday, February 3rd, 2009

ETHEX Corporation Issues Voluntary Nationwide Recall Of Prescription Prenatal and Iron Supplements To Wholesale Level

Recall Date: Tuesday, February 3rd, 2009

Ther-Rx Corporation Issues Voluntary Nationwide Recall Of Prescription Prenatal and Iron Supplements To Wholesale Level

Recall Date: Tuesday, February 3rd, 2009

Ther-Rx Corporation Issues Nationwide Voluntary Recall of Products

Recall Date: Wednesday, January 28th, 2009

ETHEX Corporation Issues Nationwide Voluntary Recall of Products

Recall Date: Wednesday, January 28th, 2009

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