Ikaria® Recalls INOMAX® DS Drug-Delivery System
Recall Date: Tuesday, August 10th, 2010
Drug Recalls and Recall Alerts | page 5
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.201 - 250 out of 300
Drug Recalls
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
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
P&G Voluntarily Recalls 4 Hour Decongestant Nasal Spray in the United States
Recall Date: Friday, June 25th, 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
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
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
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 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