Hospira Issues a Voluntary Nationwide Recall of One Lot of 0.9% Sodium Chloride Injection, USP, 100 ML, Flexible Containers Due to Particulate
Recall Date: Friday, April 26th, 2013
Drug Recalls and Recall Alerts | page 3
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.101 - 150 out of 300
Drug Recalls
Hospira Issues a Voluntary Nationwide Recall of One Lot of 0.9% Sodium Chloride Injection Due to Brass Particulates
Recall Date: Friday, March 29th, 2013
Pallimed Solutions, Inc. Announces Voluntary Nationwide Recall of All Sterile Compounded Products Dispensed
Recall Date: Tuesday, March 26th, 2013
Medprep Consulting Inc. Announces Voluntary Nationwide Recall Of All Lots Of All Compounded Products Due To Potential Mold Contamination -2
Recall Date: Wednesday, March 20th, 2013
Clinical Specialties Issues Voluntary Nationwide Recall of Avastin Unit Dose Syringes due to Potential Serious Eye Infection
Recall Date: Monday, March 18th, 2013
Affymax and Takeda Announce a Nationwide Voluntary Recall of All Lots of OMONTYS® (peginesatide) Injection
Recall Date: Saturday, February 23rd, 2013
Reumofan Plus USA, LLC and Reumofan USA, LLC is Voluntarily Recalling all lots of Reumofan Plus Tablets Due to Undeclared Drug Ingredients
Recall Date: Tuesday, February 19th, 2013
Mobius Therapeutics, LLC Issues a Voluntary Recall of Mitosol® (mitomycin for solution), 0.2 mg/vial, Kit for Ophthalmic Use
Recall Date: Thursday, January 10th, 2013
Recall - Performance Plus Marketing Press Release
Recall Date: Tuesday, December 18th, 2012
Hospira Issues Voluntary Nationwide Recall of Three Lots of Carboplatin Injection Due to Visible Particulate Matter
Recall Date: Friday, December 14th, 2012
Ameridose Issues Recall of All Products
Recall Date: Wednesday, October 31st, 2012
Body Basics Inc. Issues a Voluntary Nationwide Recall of ACTRA-Sx 500 Capsules, Lot 008-A, due to Potential Health Risks
Recall Date: Monday, September 17th, 2012
Brand New Energy Announces Voluntary Recall of Dietary Supplement EphBurn 25 Due to Possible Health Risk
Recall Date: Thursday, August 30th, 2012
Samantha Lynn Inc. Is Voluntary Recalling of all lots of Reumofan Plus Tablets Due to Undeclared Drug Ingredients
Recall Date: Tuesday, August 28th, 2012
Samantha Lynn Inc. Issues Voluntary Nationwide Recall of Reumofan Plus Tablets Due to Undeclared Drug Ingredients
Recall Date: Monday, August 27th, 2012
Hospira Announces A Nationwide Recall Of Three Lots Of Propofol Due To Glass Vial Defect
Recall Date: Thursday, August 16th, 2012
BEDFORD LABORATORIES™ ISSUES NATIONWIDE VOLUNTARY HOSPITAL/USER‐LEVEL RECALL OF LEUCOVORIN CALCIUM INJECTION
Recall Date: Thursday, July 5th, 2012
The Menz Club, LLC . Issues a voluntary nationwide recall of V-Maxx Rx due to undeclared sulfoaildenafil
Recall Date: Saturday, May 26th, 2012
Regeneca, Inc. Issues a Voluntary Nationwide Recall of All Lots of Single Capsule RegenErect Because of Potential Health Risks
Recall Date: Friday, February 24th, 2012
American Regent Initiates Nationwide Voluntary Recall Of Phenylephrine HCl Injection, USP, 1% 5 mL Vial, Lot# 0693 Due To Visible Particles
Recall Date: Thursday, February 23rd, 2012
Bedford Laboratoriesâ„¢ Issues Nationwide Voluntary Recall of Cytarabine for Injection, USP, 1 Gram per Vial
Recall Date: Thursday, February 23rd, 2012
Pedinol Pharmacal Inc. Announces Health Advisory for Gris-PEG (griseofulvin ultramicrosize) 125mg and 250mg
Recall Date: Friday, February 3rd, 2012
Bedford Laboratories Issues A Voluntary Nationwide Patient Level Recall Of Acetylcysteine Solution, USP, LOT 1877093
Recall Date: Thursday, February 2nd, 2012
