Human Science Foundation Issues Voluntary Nationwide Recall of Pro ArthMax Due to Undeclared Active Pharmaceutical Ingredients
Recall Date: Tuesday, January 14th, 2014
Drug Recalls and Recall Alerts | page 2
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.51 - 100 out of 300
Drug Recalls
Baxter Initiates Nationwide Voluntary recall Of Select Lots of Premix Parenteral Nutrition
Recall Date: Friday, January 3rd, 2014
Baxter Initiates Nationwide Voluntary Recall of One Lot of Nitroglycerin in 5% Dextrose Injection
Recall Date: Wednesday, November 27th, 2013
Deseo Rebajar Inc. Issues Voluntary Puerto Rico Recall of Adipotrim XT Due to Underclared Fluoxetine
Recall Date: Thursday, November 21st, 2013
Nephron Pharmaceuticals Corporation Announces Voluntary Recall of Albuterol Sulfate Inhalation Solution, 0.083%
Recall Date: Thursday, October 17th, 2013
Hospira Issues A Voluntary Nationwide Recall Of One Lot Of 1% Lidocaine HCL Injection Due To The Presence Of Dark Particulate
Recall Date: Friday, October 4th, 2013
H&H Medical Corporation Issues Nationwide Recall of Emergency Cricothyrotomy Kit
Recall Date: Friday, October 4th, 2013
Haute Health, LLC Conducts Voluntary Nationwide Recall of All Lots Of Virilis Pro, PHUK And Prolifta Capsules Due To Undeclared Ingredients
Recall Date: Monday, September 30th, 2013
Baxter Initiates Voluntary Recall of Two Lots of Dual Luer Lock Caps
Recall Date: Thursday, September 19th, 2013
HeartSine Technologies, Ltd. Issues Global Correction of Samaritan® 300/300P PAD
Recall Date: Monday, September 16th, 2013
Park Compounding: Sterile Medication Recall - Concerns of Sterility Assurance at Testing Vendor
Recall Date: Tuesday, September 10th, 2013
Avella Specialty Pharmacy Issues Voluntary Nationwide Recall of Two Medications Due to Concerns of Sterility Assurance at Testing Vendor
Recall Date: Monday, September 9th, 2013
Hospira Issues A Voluntary Nationwide Recall Of One Lot Of Aminosyn II 10 percent, Sulfite-Free, Due To Foreign Particulate Matter
Recall Date: Friday, August 30th, 2013
JCB Laboratories Issues Voluntary Recall of Six Drug Product Lots Due to Concerns of Sterility Assurance at Testing Vendor
Recall Date: Tuesday, August 27th, 2013
Covidien Initiates a Voluntary Recall of Certain Lots of Monoject Prefill Flush Syringes Sold in the United States and Bermuda
Recall Date: Monday, August 19th, 2013
Hospira Issues Important Safety Information for Blood Sets
Recall Date: Tuesday, August 13th, 2013
Specialty Compounding, LLC Issues Nationwide Voluntary Recall of All Lots of Unexpired Sterile Products Due to Reports of Adverse Events
Recall Date: Saturday, August 10th, 2013
Health and Beyond LLC Issues Voluntary Nationwide Recall of Tranquility Product Due to Product Having Traces of Pharmaceutical Ingredients
Recall Date: Wednesday, August 7th, 2013
Hardmenstore.com Issues Voluntary Nationwide Recall of Silver Sword and Clalis at the Request of the FDA
Recall Date: Monday, July 15th, 2013
Advance Pharmaceutical Inc. Issues Voluntary Recall of One Lot of Enteric Coated Aspirin Tablets, 81 mg, Due to Health Risk
Recall Date: Wednesday, June 19th, 2013
Fresenius Kabi USA Initiates Voluntary Recall of Single Lot of Magnesium Sulfate
Recall Date: Wednesday, May 29th, 2013
Main Street Family Pharmacy, LLC Issues Voluntary Nationwide Recall of All Sterile Compounded Products
Recall Date: Tuesday, May 28th, 2013
Pentec Health Announces Limited Voluntary Recall of Certain Compounded Prescription Therapies for Renal Patients
Recall Date: Friday, May 17th, 2013
Symbios Medical Products Issues Nationwide Recall of GOPump and GOBlock Kits
Recall Date: Thursday, May 16th, 2013
XYMOGEN identifies allergen oversight by third-party manufacturer; issues recall of artriphen™
Recall Date: Wednesday, May 8th, 2013