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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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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

FDA Awaits Court's Entry of A Permanent Injunction Against Actavis Totowa, LLC

Recall Date: Friday, January 9th, 2009

KV Pharmaceutical Voluntarily Suspends All Shipments of its Approved Tablet-form Drugs

Recall Date: Tuesday, December 23rd, 2008

ETHEX Corporation Initiated Nationwide Voluntary Recall of a Single Lot of Hydromorphone HCl 2 mg Tablets Due to Potential for Oversized Tablet

Recall Date: Tuesday, December 23rd, 2008

Hospira Issues Voluntary Recall of One Lot of 20meq Potassium Chloride in 5% Dextrose and 0.45% Sodium Chloride Injection, USP Due to Incorrect Bar Code Label

Recall Date: Monday, December 8th, 2008

ETHEX Corporation Initiated Nationwide Voluntary Recalls of Specific Lots of Five Generic Products Due to the Potential for Oversized Tablets

Recall Date: Friday, November 7th, 2008

FDA Seizes Contaminated Heparin from a Cincinnati Manufacturer

Recall Date: Thursday, November 6th, 2008

ETHEX Corporation Voluntarily Recalls Three Lots of Dextroamphetamine Sulfate 5mg Tablets Due to the Potential for Oversized Tablets

Recall Date: Wednesday, October 15th, 2008

Actavis Totowa Announces Voluntary Recall at the Retail Level of All Drug Products Manufactured at its Little Falls, New Jersey Facility

Recall Date: Friday, August 1st, 2008

EG Labs Announces Urgent Nationwide Voluntary Recall of ALL LOTS of Viapro 375 mg Capsules, due to a Potentially Harmful Ingredient

Recall Date: Wednesday, July 23rd, 2008

Firm Recall/State Recall

Recall Date: Monday, July 14th, 2008

ETHEX Corporation Voluntarily Recalls Specific Lots of 30 mg. and 60 mg. Morphine Sulfate Extended Release Tablets Due to the Potential for Oversized Tablets NDC #58177-320-04 & 58177-330-04 Lot Numbers listed below

Recall Date: Friday, June 13th, 2008

ETHEX Corporation Voluntarily Recalls a Single Lot of Morphine Sulfate 60 mg Extended Release Tablets Due to the Potential for Oversized Tablets

Recall Date: Friday, June 13th, 2008

Leiner Health Products Issues Allergy Alert on Undeclared Allergens in Liquimax� Multivitamin

Recall Date: Friday, June 6th, 2008

Medicis Announces Voluntary Recall of Solodyn� (minocycline HCL, USP) 90 Mg Tablets, Extended Release; Lot Numbers B080037 and B080038 Due to Product Mix-Up

Recall Date: Friday, May 16th, 2008

Actavis Totowa (formerly known as Amide Pharmaceutical, Inc.) recalls all lots of Bertek and UDL Laboratories Digitek (digoxin tablets, USP) as precaution

Recall Date: Friday, April 25th, 2008

Counterfeit Liviro3 Discovered After Voluntary Recall Announcement

Recall Date: Monday, January 29th, 2007

Alcon Announces Voluntary Recall of Systane� Free LIQUID GEL Lubricant Eye Drops in the United States, Including Puerto Rico

Recall Date: Thursday, December 14th, 2006

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