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News Daily News

Wingman35 Crossing Catheters Recalled Due to Tip Splitting, Separation

Todd Neale
Todd Neale
May 04, 2017
News Daily News

FDA: Class I Recall for Over 47,000 HeartStart MRx Monitor/Defibrillator Units

L.A. McKeown
L.A. McKeown
March 24, 2017
News Daily News

FDA Announces Recall of Bard’s Halo One Peripheral Vascular Guiding Sheath

L.A. McKeown
L.A. McKeown
January 31, 2017
News Daily News

FDA: Class I Recall for FindrWIRZ Guidewire System

Shelley Wood
Shelley Wood
November 22, 2016
News Daily News

FDA Classifies Latest HeartWare VAD Recalls as Class I

Michael O'Riordan
Michael O'Riordan
October 24, 2016
News Daily News

Recall Underway for AED Electrodes With Compatibility Problems

Todd Neale
Todd Neale
October 17, 2016
News Daily News

FDA: ROCKET AF Results Not Affected by Faulty INR Testing in Warfarin Arm

Michael O'Riordan
Michael O'Riordan
October 11, 2016
News Daily News

Vascular Solutions Recalls Twin-Pass Dual-Access Catheters

Michael O'Riordan
Michael O'Riordan
October 06, 2016
News Daily News

FDA: Angiographic Catheter Recalled Due to Potential Tip Separation

Todd Neale
Todd Neale
July 22, 2016
News Daily News

Variability in LDL Cholesterol Linked to Impaired Cognitive Performance in the Elderly

Todd Neale
Todd Neale
July 18, 2016
News Daily News

ROCKET AF Investigators Respond to New Questions About Point-of-Care Warfarin Monitoring Device

Todd Neale
Todd Neale
July 08, 2016
News Daily News

FDA Warns of Class I Recall for HeartWare VAD Batteries

Michael O'Riordan
Michael O'Riordan
June 29, 2016
News Industry News

Voluntary Recall of Fetch™ 2 Aspiration Catheter

April 11, 2016
News Daily News

FDA Tackles Regulatory, Scientific Issues With Point-of-Care Coagulation Monitoring Devices

Todd Neale
Todd Neale
March 24, 2016
News Daily News

FDA Issues Class I Recall for Intra-Aortic Balloon Catheter and Percutaneous Insertion Kits

Michael O'Riordan
Michael O'Riordan
March 18, 2016
News Daily News

ROCKET AF Investigators: Problems With Warfarin Monitoring Device Did Not Skew Results

Todd Neale
Todd Neale
February 04, 2016
News Daily News

FDA Proposal Seeks to Shine Early Spotlight on Postmarket Device Safety Concerns

Caitlin E. Cox
Caitlin E. Cox
January 03, 2016
News Daily News

FDA Warns of Class I Recall of Chariot Guiding Sheath Used in Peripheral Procedures

Shelley Wood
Shelley Wood
December 10, 2015
News Daily News

Path to Top FDA Post Gets a Bit Rockier for Califf

Michael O'Riordan
Michael O'Riordan
December 09, 2015
News Industry News

Voluntary Recall of Chariot™ Guiding Sheath

December 09, 2015

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