Search - tctmd.com

Displaying 1 - 20 of 40

Sort: Relevancy | Date

FDA Expresses Continuing Concerns About Getinge/Maquet CV Devices

News Daily News

FDA Expresses Continuing Concerns About Getinge/Maquet CV Devices

May 08, 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

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

Another Recall Warns of Unheralded Shutdowns With Cardiosave IABPs

News Daily News

Another Recall Warns of Unheralded Shutdowns With Cardiosave IABPs

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

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

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

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

September 30, 2022

FDA Safety Communication Updates Stance on Endologix AAA Grafts

News Daily News

FDA Safety Communication Updates Stance on Endologix AAA Grafts

January 13, 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 of Batteries for Cardiosave Hybrid/Rescue IABPs: FDA

News Daily News

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

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

September 23, 2021

Medtronic Recalls Valiant Navion TEVAR Stent Grafts

News Daily News

Medtronic Recalls Valiant Navion TEVAR Stent Grafts

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

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

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

July 01, 2020

FDA: Class I Recall for Cook Medical’s CrossCath Support Catheters

News Daily News

FDA: Class I Recall for Cook Medical’s CrossCath Support Catheters

December 17, 2019

FDA: New Concerns Surface With Endologix Grafts for AAA

News Daily News

FDA: New Concerns Surface With Endologix Grafts for AAA

October 28, 2019

FDA: Class I Recall for Burst Balloons With Sapien 3 Ultra Delivery System

News Daily News

FDA: Class I Recall for Burst Balloons With Sapien 3 Ultra Delivery System

Michael O'Riordan

August 22, 2019

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.