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Displaying 1 - 20 of 48
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DETECT-AS: Alert System Increases AV Replacement in Eligible Patients
News Conference News ACC 2025

DETECT-AS: Alert System Increases AV Replacement in Eligible Patients

Michael O'Riordan
Michael O'Riordan
April 04, 2025
FDA Expresses Continuing Concerns About Getinge/Maquet CV Devices
News Daily News

FDA Expresses Continuing Concerns About Getinge/Maquet CV Devices

Todd Neale
Todd Neale
May 08, 2024
Evoque and Patisiran: A Tale of Two Regulatory Journeys
News Opinion Off Script

Evoque and Patisiran: A Tale of Two Regulatory Journeys

Sanjay Kaul, MD
Sanjay Kaul, MD
March 29, 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
FDA: Class I Recall for Left-Sided Impella Pumps Due to TAVI Interaction
News Daily News

FDA: Class I Recall for Left-Sided Impella Pumps Due to TAVI Interaction

Caitlin E. Cox
Caitlin E. Cox
July 27, 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
FDA Alert: Possible Early Deterioration of Abbott Trifecta SAVR Valves
News Daily News

FDA Alert: Possible Early Deterioration of Abbott Trifecta SAVR Valves

Todd Neale
Todd Neale
February 27, 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
FDA: Endologix AAA Grafts Get New Labeling That Addresses Endoleak Potential
News Daily News

FDA: Endologix AAA Grafts Get New Labeling That Addresses Endoleak Potential

L.A. McKeown
L.A. McKeown
December 06, 2022
LivaNova Recalls Some LifeSPARC Controllers Used in Advanced Circulatory Support
News Daily News

LivaNova Recalls Some LifeSPARC Controllers Used in Advanced Circulatory Support

L.A. McKeown
L.A. McKeown
September 30, 2022
FDA Safety Communication Updates Stance on Endologix AAA Grafts
News Daily News

FDA Safety Communication Updates Stance on Endologix AAA Grafts

L.A. McKeown
L.A. McKeown
January 13, 2022
Fluid Leaks Spark Recall of Cardiosave Hybrid, Rescue IABPs
News Daily News

Fluid Leaks Spark Recall of Cardiosave Hybrid, Rescue IABPs

Todd Neale
Todd Neale
December 22, 2021
Class I Recall of Batteries for Cardiosave Hybrid/Rescue IABPs: FDA
News Daily News

Class I Recall of Batteries for Cardiosave Hybrid/Rescue IABPs: FDA

Caitlin E. Cox
Caitlin E. Cox
October 29, 2021
Class I Recall for Cordis’ Super Torque Catheters with Radiopaque Markers
News Daily News

Class I Recall for Cordis’ Super Torque Catheters with Radiopaque Markers

Michael O'Riordan
Michael O'Riordan
September 23, 2021
TCTMD’s Top 10 Most Popular Stories for April 2021
News Opinion Editor's Corner

TCTMD’s Top 10 Most Popular Stories for April 2021

Caitlin E. Cox
Caitlin E. Cox
May 03, 2021
Medtronic Recalls Valiant Navion TEVAR Stent Grafts
News Daily News

Medtronic Recalls Valiant Navion TEVAR Stent Grafts

Shelley Wood
Shelley Wood
February 17, 2021
FDA Reminder: Yearly, Lifelong Surveillance Needed for Endologix AAA Grafts
News Daily News

FDA Reminder: Yearly, Lifelong Surveillance Needed for Endologix AAA Grafts

L.A. McKeown
L.A. McKeown
December 04, 2020
Lotus Edge TAVR Device Recalled and Discontinued Worldwide
News Daily News

Lotus Edge TAVR Device Recalled and Discontinued Worldwide

Michael O'Riordan
Michael O'Riordan
November 18, 2020
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

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