Heartware International Recalls Certain Older Heartware Clinical Trial Controllers
Recall Date: Friday, February 27th, 2015
Medical Device Recalls and Recall Alerts
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.1 - 50 out of 211
Medical Device Recalls
Alere Initiates Voluntary URGENT CORRECTION for Use of Alere INRatio and INRatio2 PT/INR Monitor System
Recall Date: Monday, December 8th, 2014
Heart Sync Inc. Issues a Voluntary Device Correction for Multi-function Defibrillation Electrodes
Recall Date: Wednesday, December 3rd, 2014
CONMED Corporation Issues a Voluntary Device Correction for PadPro and R2 Multi-function Defibrillation Electrodes
Recall Date: Wednesday, November 26th, 2014
Customed, Inc. Issues Recall of Sterile Convenience Kits-Trays, Bags, and New Lots Added to the Previous Recall
Recall Date: Tuesday, November 25th, 2014
Covidien Initiates Voluntary Field Safety Alert for Medi-Trace™ Cadence and Kendall™ Multi-function Defibrillation Electrodes
Recall Date: Saturday, October 11th, 2014
Solace International, Inc. Issues Voluntary Nationwide Recall of Dermatend Original and Dermatend Ultra Due to Safety Concerns
Recall Date: Friday, August 29th, 2014
UPDATED: CloverSnare™ 4-Loop Vascular Retrieval Snare Recall
Recall Date: Wednesday, August 27th, 2014
Customed, Inc. Issues Recall of Sterile Convenience Surgical Packs
Recall Date: Monday, August 25th, 2014
Baxter Voluntarily Initiates U.S. Recall of Two Lots of Peritoneal Dialysis Solution Due to Presence of Particulate Matter
Recall Date: Thursday, August 14th, 2014
Vascular Solutions, Inc. Issues Recall of Langston Dual Lumen Catheters
Recall Date: Tuesday, July 8th, 2014
NDC Implements Voluntary Recall of the Hydrofinity™ Hydrophilic Guidewire
Recall Date: Wednesday, June 18th, 2014
Ventlab, LLC. Issues a Nationwide Recall of Ventlab Resuscitator Bags Due to Possible Health Risk
Recall Date: Friday, May 16th, 2014
Alere Initiates Voluntary URGENT PRODUCT RECALL of Alere INRatio 2 PT/INR Professional Test Strips
Recall Date: Tuesday, May 6th, 2014
Hospira Announces Urgent Nationwide Medical Device Correction For Gemstar Docking Station
Recall Date: Friday, May 2nd, 2014
Covidien Implements Voluntary Recall of its Pipeline™ Embolization Device and Alligator™ Retrieval Device
Recall Date: Friday, April 11th, 2014
Dräger Issues Voluntary Nationwide Recall of Optional PS500 Power Supply for Evita V500 and Babylog VN500 Ventilators
Recall Date: Wednesday, April 2nd, 2014
Abbott Issues Recall of Certain Blood Glucose Monitoring Systems
Recall Date: Friday, March 14th, 2014
Greatbatch, Inc. Issues Voluntary Field Corrective Action for Standard Offset Cup Impactor
Recall Date: Tuesday, March 11th, 2014
Philips Respironics Initiates Recall of Trilogy Ventilator
Recall Date: Wednesday, February 19th, 2014
Nipro Diagnostics, Inc. Initiates Voluntary Recall of Certain TRUEbalance and TRUEtrack Blood Glucose Meters
Recall Date: Tuesday, January 7th, 2014
Voluntary Field Corrective Action Initiated for Vital Signs Device’s CO2 Multi Absorber Due to a Health Risk
Recall Date: Wednesday, January 1st, 2014
Abrams Royal Pharmacy Issues Voluntary Nationwide Recall of All Lots of Unexpired Sterile Products Due to Lack of Sterility Assurance
Recall Date: Thursday, December 19th, 2013
Abbott Issues Voluntary Recall of Certain FreeStyle® and FreeStyle Lite® Blood Glucose Test Strips in the United States
Recall Date: Wednesday, November 27th, 2013
CLR Medicals International Inc. Issues Nationwide Recall of Viscoelastic Products
Recall Date: Monday, November 25th, 2013
Dräger issues an update on its voluntary recall of Fabius anesthesia machines
Recall Date: Tuesday, October 8th, 2013
ForeCYTE Breast Health Test; Mammary Aspiration Specimen Cytology Test (MASCT)
Recall Date: Friday, October 4th, 2013
Voluntary Recall of Specified Lots of Nova Max® Glucose Test Strips
Recall Date: Monday, July 29th, 2013
Medtronic Issues Medical Device Notifications Regarding The Synchromed Implantable Infusion System
Recall Date: Friday, June 28th, 2013
Respironics California, Inc. Recall of V60 Ventilator Designated Class I by FDA
Recall Date: Thursday, June 27th, 2013
Covidien Issues Voluntary Recall of Power Pac Batteries for Newport™ HT70 and HT70 Plus Ventilators
Recall Date: Thursday, April 18th, 2013
Abbott Initiates Voluntary Recall of FreeStyle lnsulinx® Blood Glucose Meters in the United States
Recall Date: Wednesday, April 17th, 2013
FDA Classifies Voluntary Shapematch® Cutting Guides Recall as Class I Recall
Recall Date: Wednesday, April 10th, 2013
Ad-Tech Medical Instrument Corporation Issues Global Recall of Macro Micro Subdural Electrodes
Recall Date: Thursday, February 28th, 2013
Zimmer Spine Issues Urgent Worldwide Medical Device Recall Of The Inserter Instrument For The PEEK Ardis Interbody Spacer
Recall Date: Thursday, December 20th, 2012
Bunnell Incorporated Issues Nationwide Recall Notification of Life Pulse High-Frequency Ventilator Patient Circuits
Recall Date: Wednesday, December 5th, 2012
Verathon Inc. Issues Voluntary Recall of Certain GlideScope GVL Video Laryngoscope Reusable Blades
Recall Date: Friday, November 30th, 2012
Mindray DS USA, Inc. has initiated a voluntary recall affecting the A3/A5 Anesthesia Delivery System
Recall Date: Wednesday, November 14th, 2012
HeartSine Technologies, Ltd. Issues Global Correction Of Samaritan® 300/300P PAD
Recall Date: Thursday, October 25th, 2012
Ventlab Corporation Issues Nationwide Recall of its Manual Resuscitators
Recall Date: Friday, October 19th, 2012
Accutron, Inc. Issues Nationwide Voluntary Recall of Ultra PC% Cabinet Mount Flowmeters
Recall Date: Friday, October 5th, 2012