Hospira Issues a Voluntary Nationwide Recall of One Lot of Magnesium Sulfate in 5% Dextrose Injection Due to Incorrect Barcode Labeling
Recall Date: Friday, March 6th, 2015
Drug Recalls and Recall Alerts
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.1 - 50 out of 300
Drug Recalls
FDA Classifies Previous Covidien Field Action For Its Trellis-6 and Trellis-8 Peripheral Infusion Systems as a Class 1 Recall
Recall Date: Friday, February 13th, 2015
Hospira Issues a Voluntary Global Recall of Multiple Lots of Ketorolac Tromethamine Injection Due to Potential Particulate in Glass Vials
Recall Date: Wednesday, February 11th, 2015
Hospira Issues a Voluntary Nationwide Recall of One Lot of 0.9% Sodium Chloride Injection, USP, 250 mL Due to Particulate Matter
Recall Date: Friday, January 23rd, 2015
Hospira Announces Voluntary Worldwide Recall of 10 Lots of Mitoxantrone Due to Confirmed Subpotency and Out-Of-Specification Impurities
Recall Date: Tuesday, December 23rd, 2014
Bethel Nutritional Consulting, Inc. Issues Nationwide Voluntary Recall of SLIM-K Capsules Due to Undeclared Drug Ingredients
Recall Date: Friday, December 19th, 2014
Baxter Voluntarily Initiates U.S. Recall of Two Lots of Sodium Chloride Injection, USP Due to the Presence of Particulate Matter
Recall Date: Monday, December 15th, 2014
Baxter Initiate Voluntary Recall of One Lot of Highly COncentrated Potassium Chloride Injection In The U.S. Due to Mislabeled Overpouch
Recall Date: Friday, November 21st, 2014
Baxter Initiates Voluntary Recall of Two Lots of Intravia Containers in the U.S. and Canada
Recall Date: Friday, October 24th, 2014
Contract Packaging Resources, Inc. Issues a Voluntary Nationwide Recall of Assured Brand Naproxen Sodium Tablets due to Packaging Mix-Up
Recall Date: Tuesday, October 21st, 2014
Baxter Initiates U.S. Voluntary Recall of One Lot of Potassium Chloride Injection Due to Shipping Carton Mislabeling
Recall Date: Wednesday, September 17th, 2014
Baxter Initiates Voluntary Recall of One Lot of 0.9% Sodium Chloride Injection, USP Intravenous (IV) Solution
Recall Date: Wednesday, August 13th, 2014
Baxter Initiates Voluntary Worldwide Recall Of Four Lots Of IV Solutions Due To The Presence Of Particulate Matter
Recall Date: Wednesday, July 16th, 2014
Flawless Beauty and Skin Issues Voluntary USA Recall of Unapproved Drugs
Recall Date: Tuesday, April 29th, 2014
Hospira Announces Voluntary Nationwide Recall of One Lot of 1% Lidocaine HCI INjection, USP, Due To Visible Particulates
Recall Date: Friday, April 18th, 2014
Hospira Announces Nationwide Voluntary Recall of Seven Lots of Propofol Injectable Emulsion, USP, Due to Visible Particulates
Recall Date: Friday, April 18th, 2014
Baxter Initiates U.S. Voluntary Recall of One Lot of Peritoneal Dialysis Solution Due to Container-Closure Non-Integrity
Recall Date: Wednesday, March 5th, 2014
Ben Venue Laboratories, Inc. Issues A Voluntary Nationwide Patient Level Recall Of Acetylcysteine Solution 10%, Usp, Lot 2005479
Recall Date: Friday, February 14th, 2014
Tandem Diabetes Care Expands Voluntary Recall for Select Lots of Insulin Cartridges Used with t:slim Insulin Pump
Recall Date: Wednesday, February 12th, 2014
Stemvida International Corporation Recalls StemAlive 90 Capsules Containing Undeclared Milk
Recall Date: Friday, January 17th, 2014
Tandem Diabetes Care Initiates Voluntary Recall for Specific Lots of Insulin Cartridges Used with t:slim Insulin Pump
Recall Date: Tuesday, January 14th, 2014