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  • News (12)
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Displaying 1 - 12 of 12
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FDA Warns of Air Embolism Risk With Watchman LAAO Access Systems
News Daily News

FDA Warns of Air Embolism Risk With Watchman LAAO Access Systems

Todd Neale
Todd Neale
August 06, 2025
Device Correction Issued for HeartMate Monitor Due to Potential Pump Stoppage
News Daily News

Device Correction Issued for HeartMate Monitor Due to Potential Pump Stoppage

Todd Neale
Todd Neale
June 28, 2024
Cardiosave IABPs—Yet Again—the Subject of a Class I Recall: FDA
News Daily News

Cardiosave IABPs—Yet Again—the Subject of a Class I Recall: FDA

Caitlin E. Cox
Caitlin E. Cox
August 17, 2023
Cardiosave IABPs Recalled Again, This Time Due to Potential Electrical Problems: FDA
News Daily News

Cardiosave IABPs Recalled Again, This Time Due to Potential Electrical Problems: FDA

Michael O'Riordan
Michael O'Riordan
August 10, 2023
Another Recall Warns of Unheralded Shutdowns With Cardiosave IABPs
News Daily News

Another Recall Warns of Unheralded Shutdowns With Cardiosave IABPs

Shelley Wood
Shelley Wood
March 31, 2023
New IABP Recall: Balloon Catheter Damage Might Cause Bleeding Into Pump
News Daily News

New IABP Recall: Balloon Catheter Damage Might Cause Bleeding Into Pump

Shelley Wood
Shelley Wood
January 25, 2023
Impella RP Mortality Rate No Longer a Concern, FDA Says
News Daily News

Impella RP Mortality Rate No Longer a Concern, FDA Says

Caitlin E. Cox
Caitlin E. Cox
December 05, 2022
CMS Releases Proposed Updates for Coverage of Transcatheter MV Repair
News Daily News

CMS Releases Proposed Updates for Coverage of Transcatheter MV Repair

Todd Neale
Todd Neale
July 01, 2020
Kawasaki Link to COVID-19 in Kids Probed as UK, New York Issue Alerts
News Daily News

Kawasaki Link to COVID-19 in Kids Probed as UK, New York Issue Alerts

Shelley Wood
Shelley Wood
May 06, 2020
FDA: Class I Recall for CentriMag Circulatory Support System Motor
News Daily News

FDA: Class I Recall for CentriMag Circulatory Support System Motor

Caitlin E. Cox
Caitlin E. Cox
November 07, 2019
News Daily News

FDA Classifies Latest HeartWare VAD Recalls as Class I

Michael O'Riordan
Michael O'Riordan
October 24, 2016
News Daily News

FDA: Angiographic Catheter Recalled Due to Potential Tip Separation

Todd Neale
Todd Neale
July 22, 2016
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