Search - tctmd.com

Displaying 1 - 20 of 25

Sort: Relevancy | Date

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

August 06, 2025

FDA Expresses Continuing Concerns About Getinge/Maquet CV Devices

News Daily News

FDA Expresses Continuing Concerns About Getinge/Maquet CV Devices

May 08, 2024

Abiomed Recalls Labeling for Left-Sided Impella Pumps: FDA

News Daily News

Abiomed Recalls Labeling for Left-Sided Impella Pumps: FDA

March 21, 2024

FDA Scolds Abiomed for Not Seeking a PMA for Its Web-Based User Portal

News Daily News

FDA Scolds Abiomed for Not Seeking a PMA for Its Web-Based User Portal

October 17, 2023

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

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

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

July 27, 2023

Abiomed Recalls Certain Impella 5.5 Devices Due to Risk of Purge-Fluid Leaks

News Daily News

Abiomed Recalls Certain Impella 5.5 Devices Due to Risk of Purge-Fluid Leaks

June 05, 2023

Another Recall Warns of Unheralded Shutdowns With Cardiosave IABPs

News Daily News

Another Recall Warns of Unheralded Shutdowns With Cardiosave IABPs

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

January 25, 2023

HawkOne Directional Atherectomy System Recalled Due to Risk of Tip Breakage

News Daily News

HawkOne Directional Atherectomy System Recalled Due to Risk of Tip Breakage

January 21, 2022

Fluid Leaks Spark Recall of Cardiosave Hybrid, Rescue IABPs

News Daily News

Fluid Leaks Spark Recall of Cardiosave Hybrid, Rescue IABPs

December 22, 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

September 23, 2021

Medtronic Recalls Parts of Its HeartWare VAD System

News Daily News

Medtronic Recalls Parts of Its HeartWare VAD System

May 29, 2020

FDA Advisors Recommend CVD Event Reduction Claim for Icosapent Ethyl

News Daily News

FDA Advisors Recommend CVD Event Reduction Claim for Icosapent Ethyl

Michael O'Riordan

November 14, 2019

New Recall for Maquet/Datascope IABPs Due to Potential Battery Failure

News Daily News

New Recall for Maquet/Datascope IABPs Due to Potential Battery Failure

Marcus A. Banks

July 24, 2019

FDA: Some Tainted Losartan Must Remain on US Market to Maintain Adequate Access for Patients

News Daily News

FDA: Some Tainted Losartan Must Remain on US Market to Maintain Adequate Access for Patients

March 21, 2019

New Battery, Malfunction Issues Hit Beleaguered IABPs

News Daily News

New Battery, Malfunction Issues Hit Beleaguered IABPs

November 01, 2018

Edwards Voluntarily Recalls Cardioband ‘Anchors’ Used in Mitral and Tricuspid Repair

News Daily News

Edwards Voluntarily Recalls Cardioband ‘Anchors’ Used in Mitral and Tricuspid Repair

Michael O'Riordan

February 27, 2018

TCTMD’s Top 10 Most Popular Stories for October 2017

News Opinion Editor's Corner

TCTMD’s Top 10 Most Popular Stories for October 2017

October 29, 2017

Country

First Name

Last Name

Email

Profession

Organization

Country

CAPTCHA

This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.