News Daily News FDA: Battery, Cybersecurity Issues With ICDs and CRT-Ds Now Have Firmware Fix Todd Neale April 17, 2018
News Conference News ACC 2018 Wearable Cardioverter-Defibrillator Fails to Meet Primary Endpoint in First Randomized Trial Todd Neale March 10, 2018
News Daily News Manufacturing Defect Leads to Recall of Implanted Medtronic CRT-D Devices, ICDs Todd Neale February 27, 2018
News Daily News ICD Benefit Questioned in Patients With Chronic Kidney Disease Todd Neale February 09, 2018
News Daily News FDA Warns Certain Zoll LifeVests Might Fail to Deliver Shocks Michael O'Riordan January 17, 2018
News Conference News AHA 2017 Continuing NOACs During Device Surgery Does Not Reduce Pocket Hematoma Todd Neale November 15, 2017
News Conference News TCT 2017 One in Six Patients With LBBB Post-TAVR Develop Atrioventricular Block Michael O'Riordan October 31, 2017
News Conference News PCR London Valves 2017 Pacemakers and Paravalvular Leak With Lotus: Updates From REPRISE III Shelley Wood September 27, 2017
News Industry News Boston Scientific Announces U.S. FDA Approval for MRI Labeling on High-Voltage Devices and U.S. Launch of Resonate™ Devices with the HeartLogic™ Heart Failure Diagnostic September 25, 2017
News Daily News Permanent Pacemakers Post-TAVR Don’t Increase Adverse Event Risk: Meta-analysis Ashley Lyles August 08, 2017
News Daily News One in Four ICD Patients Need Reintervention Within 5 Years Ashley Lyles August 04, 2017
News Industry News Fewer Leads, Fewer Complications: BIOTRONIK US Launches Proven DX Technology for Heart Failure Patients July 20, 2017
News Daily News Implanted Devices May Help Determine Time and Cause of Death When Autopsy Falls Short Yael L. Maxwell June 26, 2017
News Industry News Medtronic First to Receive FDA Approval for MR-Conditional Quadripolar Cardiac Resynchronization Therapy-Pacemakers May 11, 2017
News Industry News Boston Scientific Receives U.S. FDA Approval For Resonate™ Family Of High-Voltage Devices May 09, 2017
News Daily News Permanent Pacemakers After TAVR: Model Helps Predict Individual Patient Risk With Sapien 3 L.A. McKeown April 12, 2017
Presentation A Highly Predictive Risk Model for New Permanent Pacemaker Implantation After Sapien 3 TAVR April 12, 2017
News Daily News FDA: Class I Recall for Over 47,000 HeartStart MRx Monitor/Defibrillator Units L.A. McKeown March 24, 2017
News Conference News CRT 2017 Lotus TAVR Device With Depth Guard Reduces Risk of Pacemaker Implantation Michael O'Riordan February 22, 2017
News Daily News Both Appropriate and Inappropriate ICD Shocks Prompt Substantial Use of Healthcare Resources Todd Neale February 16, 2017