Teleflex Incorporated Announces Worldwide Voluntary Recall of Arrow Select IV Tubing Sets, Accessories, and Certain Embolectomy Catheters
Recall Date: Monday, March 15th, 2010
Medical Device Recalls and Recall Alerts | page 3
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.101 - 150 out of 211
Medical Device Recalls
LifeScan Recalls Specific Lots of Consumer and Professional OneTouch® SureStep® Test Strips Due To Inaccurate
Recall Date: Friday, February 26th, 2010
BD Announces Worldwide Voluntary Recall ofBD Q-Syte™ Luer Access Devices and BD Nexiva™ Closed IV Catheter Systems
Recall Date: Tuesday, February 9th, 2010
Cardiac Science Notifies AED Customers of Voluntary Medical Device Recall
Recall Date: Tuesday, February 9th, 2010
Acacia, Inc. Announces Worldwide Voluntary Recall of IV Extension Sets with BD Q-Syte™ Luer Access Device
Recall Date: Tuesday, February 9th, 2010
FDA Announces Class I Recall of Certain Infusion Set Needles
Recall Date: Tuesday, January 26th, 2010
Nipro Medical Corporation Issues a Voluntary Recall of All GlucoPro Insulin Syringes
Recall Date: Friday, January 22nd, 2010
Hettich Centrifuges Issues a North America and Canada Recall of Plastic Hematocrit Rotors
Recall Date: Friday, January 22nd, 2010
Encompass Group Voluntarily Recalls Thermoflect Product Line
Recall Date: Monday, December 28th, 2009
Stryker Operating Room System II Surgical Navigation System - Recall
Recall Date: Friday, November 27th, 2009
Cardiovascular Systems Initiates Voluntary Recall of ViperSheathTM Sheath Introducer
Recall Date: Tuesday, November 17th, 2009
Cardiac Science Notifies AED Customers of Nationwide Voluntary Medical Device Correction
Recall Date: Saturday, November 14th, 2009
Synthes USA, Ti Synex II Vertebral Body Replacement - Class I Recall
Recall Date: Thursday, November 12th, 2009
Centurion Medical Products - Premie Pack and Meconium Pack - Recall
Recall Date: Wednesday, November 4th, 2009
Cordis Initiates Nationwide Recall of CROSSOVER™ Sheath Introducer
Recall Date: Friday, October 30th, 2009
Qualitest Pharmaceuticals Issues a Voluntary Nationwide Recall of All Accusure® Insulin Syringes
Recall Date: Tuesday, October 27th, 2009
Unomedical Issues Worldwide Recall of Certain Manual Pulmonary Resuscitators
Recall Date: Wednesday, October 7th, 2009
Philips Issues Worldwide Recall of Select Heartstart Fr2+ Automated External Defibrillators
Recall Date: Saturday, October 3rd, 2009
Penumbra Announces Worldwide Voluntary Field Removal of the Original Version of 6F Neuron 070 Delivery Catheter
Recall Date: Wednesday, September 30th, 2009
LIFEPAK CR Plus Automated External Defibrillators (Physio-Control, Inc)
Recall Date: Wednesday, September 16th, 2009
Portex Uncuffed Pediatric-Sized Tracheal Tubes (sizes 2.5, 3.0 and 3.5 mm)
Recall Date: Friday, September 11th, 2009
CONMED Corporation Announces Voluntary Recall of Certain Powered Surgical Instrument Products
Recall Date: Wednesday, September 9th, 2009
Abbott Issues Voluntary Recall of POWERSAIL® Coronary Dilatation Catheters
Recall Date: Thursday, July 30th, 2009
Carefusion Issues Update Regarding Previously Disclosed June 12, 2009 Recall of the Alaris®
Recall Date: Thursday, July 30th, 2009
Dräger Initiates a Voluntary Device Recall of Stabilet Contacts Current Users
Recall Date: Monday, July 20th, 2009
Biosite Incorporated Issues Voluntary, Nationwide Recall for Cardiac Marker Test
Recall Date: Tuesday, May 5th, 2009
Arrow International Announces Worldwide Voluntary Recall of Intra Aortic Balloon Pump (IAB) Catheters
Recall Date: Monday, April 13th, 2009
Terumo Cardiovascular Systems Issues Urgent, Nationwide/Worldwide Recall of Pediatric Arterial Cannulae
Recall Date: Monday, December 1st, 2008
Thoratec Corporation Issues Worldwide Medical Device Correction of HeartMate II Left Ventricular Assist System
Recall Date: Friday, October 24th, 2008
Sage Products Inc. Issues Voluntary Recall of 2% Chlorhexidine Gluconate Cloth Patient Preoperative Skin Preparation
Recall Date: Friday, June 27th, 2008
Medtronic Initiates Voluntary Field Actions for Selected Heparin-Coated Products Used During Cardiopulmonary Bypass
Recall Date: Wednesday, May 7th, 2008
Covidien Initiates Voluntary Recall of Pre-Filled Syringes Containing Heparin
Recall Date: Friday, March 28th, 2008
Actavis Recalls Remaining Fentanyl Patches in the US as Precaution
Recall Date: Saturday, March 1st, 2008
Baxter to Proceed with Recall of Remaining Heparin Sodium Vial Products
Recall Date: Thursday, February 28th, 2008
Actavis Recalls Certain Fentanyl Patches in the US as Precaution
Recall Date: Sunday, February 17th, 2008
PRICARA RECALLS 25 mcg/hr DURAGESIC (fentanyl transdermal system) CII PAIN PATCHES
Recall Date: Tuesday, February 12th, 2008
Baxter Issues Urgent Nationwide Voluntary Recall of Heparin 1,000 Units/ml 10 and 30ml Multi-Dose Vials
Recall Date: Friday, January 25th, 2008
B. Braun´s Supplier Prompts Voluntary Recall of All Lots and All Sizes of Pre-Filled Heparin and Normal Saline Flush Syringes
Recall Date: Friday, January 18th, 2008