Cephalon, Inc. issues a voluntary nationwide recall of Treanda® (bendamustine HCL) for Injection 25mg/Vial Due to Particulate Matter
Recall Date: Friday, January 27th, 2012
Drug Recalls and Recall Alerts | page 4
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.151 - 200 out of 300
Drug Recalls
Insight Pharmaceuticals Issues A Voluntary Nationwide Recall Of "Nostrilla Nasal Decongestant" Due To Bacterial Contamination
Recall Date: Thursday, October 20th, 2011
Phoenix Import & Distribution Announces A Recall Of Pentrexyl Forte Natural
Recall Date: Friday, May 20th, 2011
Recall of Infant and Neonatal-Sized FilterLine H Set and VitaLine H Set Sampling Lines
Recall Date: Friday, May 20th, 2011
Ortho-McNeil Neurologics Voluntarily Recalls Two Lots of TOPAMAX®
Recall Date: Thursday, April 14th, 2011
American Regent Initiates Voluntary Nationwide Recall of Bacteriostatic Sodium Chloride Injection, USP, 0.9% 30 mL Multiple Dose Vials
Recall Date: Thursday, March 17th, 2011
Upsher-Smith Laboratories Announces The Voluntary Nationwide Recall Of Jantoven® Warfarin Sodium Tablets, USP, 3mg, Due To Mislabeled Bottles
Recall Date: Thursday, February 17th, 2011
Qualitest Pharmaceuticals Issues Voluntary, Nationwide Recall Of Hydrocodone Bitartrate And Acetaminophen Tablets, USP 10 MG / 500 MG, NDC 0603-3888-20, 60 Count, Lot Numbers T150G10B, T120J10E And T023M10A And Phenobarbital Tablets, USP 32.4 MG, NDC 0603-5166-32, 1000 Count, Lot Numbers T150G10B, T120J10E And T023M10A
Recall Date: Sunday, February 6th, 2011
Watson Announces Important Action Related to Nationwide Recall of Triad Alcohol Prep Products Included in Products
Recall Date: Friday, February 4th, 2011
McNeil Consumer Healthcare Initiates Voluntary Recall Of Certain Over-The-Counter (OTC) Products
Recall Date: Friday, January 14th, 2011
Teva Pharmaceuticals, U.S.A issues a voluntary nationwide recall of Metronidazole Tablets USP, 250mg Due to Low Weight Tablets
Recall Date: Thursday, January 6th, 2011
American Regent Initiates Voluntary Recall of Dexamethasone Sodium Phosphate Injection, USP 4 mg/mL, 30 mL Multiple Dose Vial
Recall Date: Thursday, December 23rd, 2010
Reese Pharmaceutical Company Announces the Voluntary Nationwide Recall of Certain Over-The-Counter Cold Relief Products that are Mislabeled.
Recall Date: Friday, December 10th, 2010
Actavis Encourages Consumers to Return Fentanyl Transdermal System 25 mcg/h
Recall Date: Thursday, November 4th, 2010
bioMérieux, Inc. Issues Urgent Product Correction for VITEK® 2 Gram Negative Susceptibility Cards Containing Piperacillin/Tazobactam
Recall Date: Wednesday, October 27th, 2010
Actavis Inc. Issues a Voluntary Recall of 18 Lots of Fentanyl Transdermal System 25 mcg/h
Recall Date: Thursday, October 21st, 2010
Amgen Initiates Voluntary Nationwide Recall Of Certain Lots Of Epogen® And Procrit® (Epoetin Alfa)
Recall Date: Friday, September 24th, 2010
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