News Daily News FDA Warns of Air Embolism Risk With Watchman LAAO Access Systems Todd Neale August 06, 2025
News Daily News Device Correction Issued for HeartMate Monitor Due to Potential Pump Stoppage Todd Neale June 28, 2024
News Daily News Cardiosave IABPs—Yet Again—the Subject of a Class I Recall: FDA Caitlin E. Cox August 17, 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 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 Impella RP Mortality Rate No Longer a Concern, FDA Says Caitlin E. Cox December 05, 2022
News Daily News CMS Releases Proposed Updates for Coverage of Transcatheter MV Repair Todd Neale July 01, 2020
News Daily News Kawasaki Link to COVID-19 in Kids Probed as UK, New York Issue Alerts Shelley Wood May 06, 2020
News Daily News FDA: Class I Recall for CentriMag Circulatory Support System Motor Caitlin E. Cox November 07, 2019
News Daily News FDA Classifies Latest HeartWare VAD Recalls as Class I Michael O'Riordan October 24, 2016
News Daily News FDA: Angiographic Catheter Recalled Due to Potential Tip Separation Todd Neale July 22, 2016