AM2 PAT, Inc. Issues Nationwide Recall of All Lots and All Sizes of Pre-Filled Heparin and Normal Saline Flushes
Recall Date: Friday, January 18th, 2008
Medical Device Recalls and Recall Alerts | page 4
Drug and Medical Recalls
View the list below of the latest Medical Device recall information. The majority of the recalls below originated from either the FDA or the USDA.151 - 200 out of 211
Medical Device Recalls
Cardinal Health Statement on Alaris Pump Module Worldwide Voluntary Recall
Recall Date: Thursday, December 20th, 2007
AM2 PAT, Inc. Issues Nationwide Recall of Pre-Filled Heparin Lock Flush Solution USP (5 mL in 12 mL Syringes)
Recall Date: Thursday, December 20th, 2007
B. Braun Medical Inc. Issues Nationwide Recall of Normal Saline Flush Syringes with Lot Numbers Ending in SFR
Recall Date: Friday, September 14th, 2007
Ortho-Clinical Diagnostics, Inc. Issues Voluntary, Nationwide Recall for Cardiac Marker
Recall Date: Friday, May 4th, 2007
ResMed Issues a Voluntary Recall for Certain S8 Flow Generators
Recall Date: Monday, April 23rd, 2007
Smith & Nephew Issues Nationwide Recall of RF Denervation Probes Used for the Spine
Recall Date: Monday, March 26th, 2007
Defibtech Announces a Worldwide Voluntary Recall of Lifeline and ReviveR Automated External Defibrillators
Recall Date: Tuesday, March 6th, 2007
Boston Scientific Announces Nationwide Recall of 51 Mach 1 Guide Catheters
Recall Date: Friday, December 15th, 2006
Rockline Announces Voluntary Product Withdrawal of Wet Wipes Products
Recall Date: Friday, November 17th, 2006
Endologix Announces Limited Voluntary Recall Of Visiflex 155 Mm Delivery Catheters
Recall Date: Thursday, November 9th, 2006
Roche Diagnostics Announces Nationwide Recall on Medical Device Used to Determine Blood Clotting Time
Recall Date: Thursday, October 19th, 2006
Gerber Products Company Issues Nationwide Allergy Alert on Undeclared Latex in Fashion Tint 9 Ounce Bottles (3 Packs)
Recall Date: Thursday, August 24th, 2006
Boston Scientific Announces Physician Communication Related to Products in Its CRM Group
Recall Date: Monday, June 26th, 2006
Sage Products Inc. Issues a Voluntary Recall of Comfort Shield Perineal Care Washcloths in the U.S. and Canada
Recall Date: Friday, June 23rd, 2006
MRL, Inc. a Welch Allyn Company, Issues a Voluntary Worldwide Recall of Selected AED20 Automatic External Defibrillators
Recall Date: Thursday, June 15th, 2006
Hamilton Medical Issues a Medical Device Safety Alert on certain RAPHAEL Ventilators
Recall Date: Tuesday, June 6th, 2006
Boca Medical Products, Inc. Issues Nationwide Recall of Insulin Syringe Product
Recall Date: Thursday, April 13th, 2006
Blackstone Medical, Inc. Issues Voluntary Recall of ICON Modular Fixation System
Recall Date: Wednesday, April 12th, 2006
Disetronic Medical Systems, Inc. Announces a Voluntary Nationwide Recall of all ACCU-CHEK Ultraflex Infusion Sets
Recall Date: Monday, April 3rd, 2006
Ossur Announces Voluntary Recall of Certain Models of the Total Knee
Recall Date: Wednesday, March 29th, 2006
The First Years Announces Voluntary Recall of Liquid-Filled Teethers
Recall Date: Friday, January 27th, 2006
Vapotherm ISSUES URGENT NATIONWIDE RECALL OF All Vapotherm 2000i Respiratory Gas Humidification Devices
Recall Date: Tuesday, January 24th, 2006
Roche Diagnostics Issues a Worldwide Voluntary Recall of Some of its ACCU-CHEK Aviva Meters
Recall Date: Monday, January 16th, 2006
Endologix Announces Limited Voluntary Recall of Powerlink System Delivery Catheter
Recall Date: Wednesday, December 14th, 2005
FDA Class I Classification Given to Baxter's September 2005 Urgent Product Recall for Meridian Hemodialysis Instrument
Recall Date: Tuesday, December 13th, 2005
Boston Scientific Announces Worldwide Recall of Stainless Steel Greenfield Vena Cava Filters Manufactured Before March 10, 2004
Recall Date: Friday, December 2nd, 2005
Omron 3-Way Instant Thermometers Recalled for Possible Safety Risk
Recall Date: Monday, October 24th, 2005
BioMerieux Issues Worldwide Correction Recall of VeriCal Calibrator Set
Recall Date: Thursday, October 6th, 2005
Gambro Dasco S.p.A. Issues Worldwide Safety Alert for the Prisma System
Recall Date: Tuesday, August 16th, 2005
Disetronic Medical Systems, Inc. Announces a Voluntary Recall of the D-TRON Adapters, Used With the D-TRONplus Insulin Pump
Recall Date: Friday, July 29th, 2005
Boston Scientific Announces Worldwide Recall of Hemashield VantageT Peripheral Vascular Grafts
Recall Date: Monday, June 27th, 2005
Qualitest Pharmaceuticals, Inc. Issues a Voluntary Nationwide Recall of Accusure Insulin Syringes 1cc 28 Gauge 1/2 Inch 100's
Recall Date: Tuesday, June 14th, 2005
MRL, Inc. a Welch Allyn Company Issues a Voluntary Worldwide Recall of Selected AED20 Automatic External Defibrillators
Recall Date: Tuesday, May 10th, 2005
Kingswood Laboratories, Inc. Issues Nationwide Recall of Moi-Stir Oral Swabsticks
Recall Date: Friday, April 22nd, 2005
LifeScan, Inc, Announces Worldwide Correction Concerning Certain Blood Glucose Meters
Recall Date: Wednesday, April 20th, 2005
Heartsine Technologies, Inc. Issues Worldwide Recall of Certain Automatic External Defibrillators
Recall Date: Friday, March 18th, 2005
Medtronic Announces Voluntary Recall of Certain Monophasic LIFEPAK 500 Automated External Defibrillators
Recall Date: Friday, February 25th, 2005
Medtronic Issues Notification Regarding Certain Implantable Defibrillator Models
Recall Date: Friday, February 11th, 2005
BD Statement Regarding Worldwide Voluntary Recall of BD ProbeTecT ET Urine Processing Kits
Recall Date: Friday, January 28th, 2005
Bio-Med Devices, Inc. Issues Nationwide Recall on Bio-Med Patient Tubing Assembly with Adaptor
Recall Date: Wednesday, December 8th, 2004