News Daily News FDA Warns of Air Embolism Risk With Watchman LAAO Access Systems Todd Neale August 06, 2025
News Daily News Some Mitral TEER Patients Slipping Through the Cracks in the First Month Michael O'Riordan March 21, 2025
News Daily News Class I Recall for Amplatzer LAAO's Steerable Delivery Sheath Shelley Wood July 26, 2023
News Daily News FDA Alert: Possible Early Deterioration of Abbott Trifecta SAVR Valves Todd Neale February 27, 2023
News Daily News Medical Devices Cleared on Faulty Predicates More Likely to be Recalled Michael O'Riordan January 17, 2023
News Daily News LivaNova Recalls Some LifeSPARC Controllers Used in Advanced Circulatory Support L.A. McKeown September 30, 2022
News Daily News FDA, Abbott Warn of Potential MitraClip Locking Malfunctions L.A. McKeown September 09, 2022
News Daily News Radiation Exposure ‘Extraordinarily’ High for Imagers in Structural Procedures Yael L. Maxwell July 11, 2022
News Daily News Medtronic Recalls Harmony Delivery Catheters Due to Breakage Risk L.A. McKeown April 26, 2022
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 European Regulators Approve First Transcatheter MV Replacement Device Michael O'Riordan January 30, 2020
News Daily News FDA: Class I Recall for Burst Balloons With Sapien 3 Ultra Delivery System Michael O'Riordan August 22, 2019
News Daily News Burst Balloons With Sapien 3 Ultra Prompt ‘Urgent Field Safety Notice’ and Canadian Recall Shelley Wood July 22, 2019
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 Two Pediatric Cardiac Catheters Recalled for Defective Balloons L.A. McKeown April 26, 2019