News Opinion Editor's Corner TCTMD’s Top 10 Most Popular Stories for July 2025 Caitlin E. Cox July 31, 2025
News Opinion Editor's Corner TCTMD’s Top 10 Most Popular Stories for June 2025 Michael O'Riordan June 30, 2025
News Daily News ‘Sobering’ Adverse Event Rate With Evoque Seen in Real-world Use Yael L. Maxwell June 18, 2025
News Daily News VASCADE Closure Device: FDA Database Tracks Common Complications, Deaths Caitlin E. Cox September 10, 2021
News Daily News No Harm, No Help With Bioabsorbable-Polymer Stents: Registry Michael O'Riordan March 01, 2021
News Daily News FDA Data Raise Red Flags for Suture-Based Vascular Closure Devices Caitlin E. Cox February 11, 2021
News Conference News TCT 2019 Watchman Adverse Events: Analysis Digs Into What’s Been Reported to the FDA Todd Neale October 04, 2019
News Daily News No Volume-Outcome Link With Watchman for LAA Closure? Single-Center Study Michael O'Riordan August 19, 2019
News Daily News More Acute Stent Thrombosis With Synergy Stent in Bern PCI Registry Michael O'Riordan August 14, 2019
News Conference News ACC 2019 CardioMEMS Postapproval Study Linked to Reduction in Heart Failure Hospitalizations at 1 Year Yael L. Maxwell March 20, 2019
News Conference News CRT 2019 Adverse Events Reports for Guide Extension Catheter Should Spur Cautious Use Yael L. Maxwell March 05, 2019
News Daily News CV Devices in the Fast Lane: FDA’s Approval Often Rests on Early Evidence Caitlin E. Cox September 05, 2018
News Daily News ‘The Bleeding Edge’ Documentary, Tackling Medical Device Regulation, Spurs Diverse Cardiology Reactions Yael L. Maxwell August 17, 2018
News Daily News Complications Spiked, Then Fell, After Initial Introduction of Watchman LAA Closure Device Todd Neale October 12, 2017
News Daily News Pulmonary Artery Injury More Likely With Real-World Use of CardioMEMS, Analysis Suggests Todd Neale September 19, 2017
News Conference News ESC 2017 Leaflet Thrombosis After TAVR Tied to Cardiogenic Shock and Death Yael L. Maxwell September 01, 2017
News Daily News FDA Warns of Class I Recall of Chariot Guiding Sheath Used in Peripheral Procedures Shelley Wood December 10, 2015
News Daily News La FDA Da la Voz de Alarma sobre el Uso del Dispositivo Lariat para el Cierre del AAI en Pacientes con FA Yael L. Maxwell July 17, 2015