News Daily News FDA Warns of Air Embolism Risk With Watchman LAAO Access Systems Todd Neale August 06, 2025
News Daily News Reduced Shock Efficacy With Some Boston Scientific Defibrillation Leads Todd Neale August 06, 2025
News Daily News FDA Issues Safety Communication for Some Accolade Pacemakers L.A. McKeown December 16, 2024
News Daily News Device Correction Issued for HeartMate Monitor Due to Potential Pump Stoppage Todd Neale June 28, 2024
News Opinion Off Script Evoque and Patisiran: A Tale of Two Regulatory Journeys Sanjay Kaul, MD March 29, 2024
News Daily News FDA Scolds Abiomed for Not Seeking a PMA for Its Web-Based User Portal Caitlin E. Cox October 17, 2023
News Daily News Label for Impella RP Flex Catheters Recalled to Address Anticoagulant Confusion: FDA Caitlin E. Cox August 18, 2023
News Daily News Cardiosave IABPs Recalled Again, This Time Due to Potential Electrical Problems: FDA Michael O'Riordan August 10, 2023
News Daily News Abiomed Recalls Certain Impella 5.5 Devices Due to Risk of Purge-Fluid Leaks Caitlin E. Cox June 05, 2023
News Daily News Another Recall Warns of Unheralded Shutdowns With Cardiosave IABPs Shelley Wood March 31, 2023
News Daily News New IABP Recall: Balloon Catheter Damage Might Cause Bleeding Into Pump Shelley Wood January 25, 2023
News Daily News Medical Devices Cleared on Faulty Predicates More Likely to be Recalled Michael O'Riordan January 17, 2023
News Daily News Impella RP Mortality Rate No Longer a Concern, FDA Says Caitlin E. Cox December 05, 2022
News Daily News A Simple Nudge Moves the Needle on Statin Prescribing Michael O'Riordan December 02, 2022
News Daily News FDA: New Fix Available for Medtronic’s Troubled HeartWare VADs Michael O'Riordan October 17, 2022
News Daily News LivaNova Recalls Some LifeSPARC Controllers Used in Advanced Circulatory Support L.A. McKeown September 30, 2022
News Daily News FDA: Class I Recall of Cobalt and Crome ICDs and CRT-Ds Due to Reduced-Energy Shock L.A. McKeown August 19, 2022