Respironics California, Inc., Voluntary Recall Notification Of A Limited Number Of Respironics V60 Ventilators
Recall Date: Friday, August 31st, 2012
Medical Device Recalls and Recall Alerts | page 2
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.51 - 100 out of 211
Medical Device Recalls
Covidien Implements a Voluntary Recall of Certain Lots of Shiley Adult Tracheostomy Tubes
Recall Date: Saturday, August 4th, 2012
CareFusion Provides Update On Voluntary Recall Of EnVe Ventilator
Recall Date: Wednesday, July 18th, 2012
CareFusion Provides Update On Voluntary Recall Of Select AirLife™ Respiratory Products
Recall Date: Tuesday, July 3rd, 2012
Nidek Medical Products, Inc. issues an Urgent Medical Device Correction affecting oxygen concentrators
Recall Date: Tuesday, June 19th, 2012
Flight Medical Innovations Ltd. Provides Update on Recall of Ventilator Remote Alarm Cable
Recall Date: Tuesday, February 14th, 2012
Carefusion Provides Update on Voluntary Recall of Neurilogical Monitoring Software and Devices
Recall Date: Friday, January 20th, 2012
Covidien Contraindicates the Use of Duet TRS for Thoracic Surgery, Implements a Voluntary Recall
Recall Date: Wednesday, January 18th, 2012
Smiths Medical Issues Urgent Ddevice Recall of Certain Bivona® Neonatal, Pediatric, and Fflextend Tracheostomy Tubes
Recall Date: Tuesday, December 27th, 2011
IKARIA® Issues Notice of Completed Remediation For INOMAX® DS Drug-Delivery System
Recall Date: Friday, December 23rd, 2011
CareFusion Provides Update on Previously Announced Ventilator Recall
Recall Date: Thursday, December 22nd, 2011
American Regent, Inc. Initiates Voluntary Recall of Seventeen Lots of Vasopressin Injection, USP, Multiple Dose Vials due to Sub-Potency
Recall Date: Wednesday, August 3rd, 2011
Global Focus Marketing & Distribution, Ltd. Recalls The Silencer® S2200 Centrifuge
Recall Date: Tuesday, July 19th, 2011
Churchill Medical Systems, A Vygon Company, Skin-Prep Wipes used in Convenience Kits
Recall Date: Friday, June 3rd, 2011
Moog Recalls Curlin Ambulatory Infusion Pump Models 6000 CMS, 6000 CMS IOD, PainSmart, and PainSmart IOD
Recall Date: Monday, April 11th, 2011
CDC And ADPH Investigate Outbreak At Alabama Hospitals; Products Recalled
Recall Date: Wednesday, March 30th, 2011
APP Pharmaceuticals Issues A Nationwide Voluntary Recall Of Irinotecan Hydrochloride Injection
Recall Date: Sunday, March 27th, 2011
Millar Instruments, Inc. Issues a Recall of Millar Mikro-Tip Angiographic Catheter, Model SPC-454D and SPC-454F
Recall Date: Tuesday, March 22nd, 2011
Lilly Announces Important Action Regarding Recall of Alcohol Prep Pads Made by Triad Group Included in Forteo Starter Kits
Recall Date: Friday, March 18th, 2011
OTC DRUG Nationwide Recall--Important information for patients about IV PREP Antiseptic Wipes
Recall Date: Monday, March 7th, 2011
Roche Insulin Delivery Systems announces recall of ACCU-CHEK® FlexLink Plus infusion sets
Recall Date: Thursday, February 24th, 2011
Cumberland Pharmaceuticals Announces Voluntary Recall of Acetadote® Vials
Recall Date: Saturday, January 1st, 2011
ev3 Initiates Voluntary Recall of Specific Lots of NanoCross™ .014" OTW PTA Dilatation Catheter
Recall Date: Tuesday, December 28th, 2010
Advanced Bionics Announces Voluntary Recall Of The Hires 90k Cochlear Implant
Recall Date: Wednesday, November 24th, 2010
WalkMed Infusion Issues Nationwide Recall of Triton Pole Mount Infusion Pumps
Recall Date: Wednesday, November 24th, 2010
WalkMed Infusion Issues Nationwide Recall of Triton Infusion Pump
Recall Date: Friday, November 5th, 2010
Carefusion Recall of Alaris PC Units Model 8015 Classified as Class I Recall
Recall Date: Friday, November 5th, 2010
FDA Classifies Previous Field Action of Medtronic Surgical Device as Class I Recall
Recall Date: Monday, November 1st, 2010
Westmed, Inc. Issues Nationwide Recall of BagEasy Manual Resuscitation Devices
Recall Date: Wednesday, September 15th, 2010
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
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
Covidien Initiates Voluntary Recall of Certain Shiley™ Tracheostomy Tubes
Recall Date: Friday, April 23rd, 2010