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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

April 04, 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

June 28, 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

Label for Impella RP Flex Catheters Recalled to Address Anticoagulant Confusion: FDA

News Daily News

Label for Impella RP Flex Catheters Recalled to Address Anticoagulant Confusion: FDA

August 18, 2023

Impella RP Mortality Rate No Longer a Concern, FDA Says

News Daily News

Impella RP Mortality Rate No Longer a Concern, FDA Says

December 05, 2022

FDA: Medtronic Stops Production and Distribution of Troubled HeartWare VAD

News Daily News

FDA: Medtronic Stops Production and Distribution of Troubled HeartWare VAD

June 03, 2021

FDA: Class I Recall for HeartWare VAD Pump Implant Kit

News Daily News

FDA: Class I Recall for HeartWare VAD Pump Implant Kit

March 01, 2021

FDA Expands TAVR Indication to Low-Risk Patients

News Daily News

FDA Expands TAVR Indication to Low-Risk Patients

Michael O'Riordan

August 16, 2019

Class I Recall for Medtronic’s HeartWare HVAD System

News Daily News

Class I Recall for Medtronic’s HeartWare HVAD System

Michael O'Riordan

June 04, 2018

News Daily News

HeartMate 3 Problem With Outflow Graft Twisting Called Class I Recall by FDA

May 23, 2018

News Daily News

HeartMate II Left Ventricular Assist System Under Recall Due to Controller Exchange Problems

May 24, 2017

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