News Daily News FDA: Class I Recall for Left-Sided Impella Pumps Due to TAVI Interaction Caitlin E. Cox July 27, 2023
News Daily News Lotus Edge TAVR Device Recalled and Discontinued Worldwide Michael O'Riordan November 18, 2020
News Daily News CMS Releases Proposed Updates for Coverage of Transcatheter MV Repair Todd Neale July 01, 2020
News Daily News Terumo’s Solopath Transfemoral System and Recollapsible Balloon Access System Recalled for Dislodging Issues L.A. McKeown May 30, 2019
News Daily News Boston Scientific Recalls All Lotus Valves, Including Lotus With Depth Guard Michael O'Riordan February 23, 2017
News Daily News Boston Scientific Announces Fix for Lotus Edge TAVR Device Following Implantation ‘Pause’ L.A. McKeown January 11, 2017
News Daily News Under Surveillance: Ballooning Numbers, Better Survival, Lower-Risk Patients in Latest TVT Registry Data L.A. McKeown December 13, 2016
News Daily News Bajo Vigilancia: Cifras Infladas, una Mejor Supervivencia y Pacientes de Menor Riesgo en los Últimos Datos del Registro TVT L.A. McKeown December 13, 2016
News Daily News Medtronic Warns of Vascular Trauma, Some Resulting in Death, With CoreValve’s EnVeo R Delivery Catheter Michael O'Riordan August 18, 2016
News Daily News Experimental FAAH Inhibitors Do Not Pose Safety Risk, FDA Concludes Michael O'Riordan August 12, 2016