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Medical Device Recalls

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.

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Integra Issues URGENT Worldwide Recall of NeuroBalloonTM Catheter

Recall Date: Tuesday, August 24th, 2010

Airgas South Initiates Precautionary Voluntary Recall of Medical Gas Products at Chattanooga, TN Facility

Recall Date: Monday, July 26th, 2010

Cook Initiates Voluntary Recall of Certain Ciaglia Blue Rhino and Ciaglia Blue Dolphin Percutaneous Tracheostomy Introducer Sets and Trays that Contain a Covidien 6PERC or 8PERC Shiley™ Tracheostomy Tube

Recall Date: Wednesday, July 21st, 2010

Defibtech Announces a Voluntary Recall of DBP-2800 Battery Packs used in the Lifeline AED® and ReviveR AEDTM

Recall Date: Tuesday, June 8th, 2010

Sagent Pharmaceuticals Initiates a Nationwide Voluntary Recall of All Lots of Metronidazole Injection, USP 500 mg/100 mL

Recall Date: Monday, May 17th, 2010

Teleflex Medical Announces Worldwide Voluntary Recall of Teleflex Medical AQUA+FLEX Hygroscopic Condenser Humidifier (Catalog Number 1570)

Recall Date: Thursday, May 6th, 2010

Covidien Initiates Voluntary Recall of Certain Shiley™ Tracheostomy Tubes

Recall Date: Friday, April 23rd, 2010

Teleflex Incorporated Announces Worldwide Voluntary Recall of Arrow Select IV Tubing Sets, Accessories, and Certain Embolectomy Catheters

Recall Date: Monday, March 15th, 2010

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

Cardiovascular Systems ViperSheath 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

Qualitest Pharmaceuticals, Inc. Issues a Voluntary Nationwide Recall of Accusure® Insulin Syringes (1/2 Cc - 31 G - Short Needle) Lot #6jcb1 and Accusure® Insulin Syringes (1 Cc - 31 G - Short Needle) Lot #7cpt1

Recall Date: Friday, August 21st, 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

Roche Diagnostics notifies customers of the potential for ACCU-CHEK® Softclix 10 and/or 17 count lancets to be uncapped which may lead to an accidental needle stick

Recall Date: Sunday, May 17th, 2009

Biosite Incorporated Issues Voluntary, Nationwide Recall for Cardiac Marker Test

Recall Date: Tuesday, May 5th, 2009

Disetronic Medical Systems Inc. (a member of the Roche Group) announces a recall (field corrective action) of the ACCU-CHEK� Spirit insulin pump due to �up� and/or �down� button failures

Recall Date: Thursday, April 30th, 2009

Arrow International Announces Worldwide Voluntary Recall of Intra Aortic Balloon Pump (IAB) Catheters

Recall Date: Monday, April 13th, 2009

Castillo Issues Urgent Nationwide Voluntary Recall Of Monell�s Teething Cordial / 4,100 Units / Named In Spanish "Cordial De Monell Para La Denticion" Bar Code 7460840410019

Recall Date: Wednesday, April 8th, 2009

FDA Classifies Medtronic Voluntary February Recall for BioGlide� Ventricular Snap Shunt Catheters (Models 27782, 27708 and 27802) as Class I

Recall Date: Friday, March 27th, 2009

FDA: Insulin Pens and Insulin Cartridges Must Not Be Shared

Recall Date: Thursday, March 19th, 2009

FDA Warns About Risk of Wearing Medicated Patches During MRIs

Recall Date: Thursday, March 5th, 2009

FDA Announces Class I Recall of Ophthalmic Surgical Device

Recall Date: Friday, January 2nd, 2009

Firm Recall/State Recall

Recall Date: Tuesday, December 23rd, 2008

FDA Announces Class I Recalls of Two Unapproved Devices

Recall Date: Monday, December 15th, 2008

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

Atrium Initiates Voluntary Recall Action Regarding HYDRAGLIDE� Brand Heparin-Coated Thoracic Drainage Catheters used for Autotransfusion during Cardiopulmonary Bypass Surgery

Recall Date: Monday, May 12th, 2008

Medtronic Initiates Voluntary Field Actions for Selected Heparin-Coated Products Used During Cardiopulmonary Bypass

Recall Date: Wednesday, May 7th, 2008

106 total items found
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