Medicine Recalls

Description	Publish Date
Zyprexa Relprevv (Olanzapine Pamoate): Drug Safety Communication - FDA Investigating Two Deaths Following Injection	6/18/2013 4:00:00 PM
Endologix, Inc. AFX Introducer System: Class 1 Recall - Reports Of Dilator Breaking During Procedures	6/18/2013 2:30:00 PM
Cybersecurity for Medical Devices and Hospital Networks: FDA Safety Communication	6/17/2013 6:27:00 PM
MedWatch May 2013 drug safety labeling changes	6/13/2013 10:15:00 PM
Warfarin 2 mg Tablets by Zydus Pharmaceuticals USA Inc.: Recall - Due to Oversized Tablets	6/12/2013 10:23:00 PM
Symbios GOPump and GOBlock Kits: Class 1 Recall - Potential for Excessive High Flow Rates	6/12/2013 9:30:00 PM
Bethel Nutritional Consulting, Inc. Bethel 30: Recall: Undeclared Drug Ingredient.	6/11/2013 8:00:00 PM
Vecuronium Bromide For Injection by Sagent Pharmaceuticals, Inc.: Recall - Elevated Impurity Result Detected	6/10/2013 8:00:00 PM
Nephron Pharmaceuticals Corp. EZ Breathe Atomizer: Class 1 Recall - Washer Could Become Dislodged	6/3/2013 7:05:00 PM
Olympia Pharmacy Sterile Compounded Products: Recall - Concerns About Sterility Assurance	5/30/2013 7:40:00 PM
Magnesium Sulfate: Drug Safety Communication - Recommendation Against Prolonged Use in Pre-term Labor	5/30/2013 7:00:00 PM
Magnesium Sulfate Injection by Fresenius Kabi USA: Recall - Glass Particles in Vials	5/29/2013 4:55:00 PM
Main Street Family Pharmacy in Tennessee: FDA Alerts Health Care Providers of Adverse Reactions Associated with Steroid Injections	5/24/2013 6:06:00 PM
Cook Medical, Inc Zilver PTX Drug-Eluting Peripheral Stent: Class 1 Recall - Complaints of Delivery System Tip Separation	5/24/2013 3:30:00 PM
Methotrexate Sodium, USP Injectable Vials by Sandoz US: Recall - Particulate Matter In Vials	5/21/2013 10:05:00 AM
Abbott Diabetes Care: Class 1 Recall - FreeStyle InsuLinx Blood Glucose Meters - Risk of Incorrect Test Result	5/20/2013 6:00:00 PM
All Sterile Drug Products Made and Distributed By NuVision Pharmacy Dallas Facility: Recall - Lack Of Sterility Assurance	5/18/2013 7:51:00 PM
Compounded Prescription Therapies By Pentec Health Inc.: Recall - Lack Of Sterility Assurance	5/17/2013 7:55:00 PM
Atriphen dietary supplement (Xymogen brand): Recall - Potential Allergic Reaction Due to Milk and Soy	5/9/2013 8:00:00 PM
The Compounding Shop: FDA News Release - Lack of Sterility Assurance of Drug Products	5/8/2013 9:45:00 PM
SexVoltz, Velextra, and Amerect by Beomonstar Products: Recall - Undeclared Drug Ingredient	5/8/2013 1:30:00 PM
Bullet Proof: Public Notification - Undeclared Drug Ingredient	5/7/2013 9:30:00 PM
Lightning Rod Capsules: Recall - Undeclared Drug Ingredient	5/7/2013 9:15:00 PM
Maquet SERVO-i Ventilator Battery Module: Class 1 Recall - Battery Run Time Shorter Than Expected	5/7/2013 8:45:00 PM
Medtronic: Class 1 Recall - Medtronic Deep Brain Stimulation Lead Kit and Activa Dystonia HDE Kit	5/7/2013 6:30:00 PM

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