Search - tctmd.com

Displaying 1 - 20 of 24

Sort: Relevancy | Date

FDA Panel Declines to Endorse Ventura Interatrial Shunt for HFrEF

News Daily News

FDA Panel Declines to Endorse Ventura Interatrial Shunt for HFrEF

December 05, 2025

FDA Approves Dropping Aspirin for HeartMate 3 LVAD Patients

News Daily News

FDA Approves Dropping Aspirin for HeartMate 3 LVAD Patients

August 21, 2024

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

HeartMate 3 Recalled for Risk of Blood Leaks or Air in System

News Daily News

HeartMate 3 Recalled for Risk of Blood Leaks or Air in System

May 15, 2024

HeartMate II and 3 LVADs Recalled Due to Potential for Outflow Graft Obstruction

News Daily News

HeartMate II and 3 LVADs Recalled Due to Potential for Outflow Graft Obstruction

April 22, 2024

New Risk Score Better for Capturing Medical Urgency for Heart Transplantation

News Daily News

New Risk Score Better for Capturing Medical Urgency for Heart Transplantation

Michael O'Riordan

February 19, 2024

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

Journal Series Explores How Eroding Abortion Access Impacts the HF Community

News Daily News

Journal Series Explores How Eroding Abortion Access Impacts the HF Community

June 15, 2023

Monitoring PA Pressures With CardioMEMS May Help LVAD Patients

News Daily News

Monitoring PA Pressures With CardioMEMS May Help LVAD Patients

April 27, 2023

For Some, Hopes for a Heart Grow Dim as LVAD-Only Centers Spread

News Daily News

For Some, Hopes for a Heart Grow Dim as LVAD-Only Centers Spread

Michael O'Riordan

January 30, 2023

Cardiogenic Shock Outcomes Markedly Worse in De Novo HF Patients

News Daily News

Cardiogenic Shock Outcomes Markedly Worse in De Novo HF Patients

December 09, 2022

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

Novel Interatrial Shunt Shows Promise at 1 Year in HF Patients With Reduced and Preserved EF

News Daily News

Novel Interatrial Shunt Shows Promise at 1 Year in HF Patients With Reduced and Preserved EF

November 02, 2018

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

FDA Grants HeartWare LVAD a Destination Therapy Indication

News Daily News

FDA Grants HeartWare LVAD a Destination Therapy Indication

September 28, 2017

News Daily News

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

May 24, 2017

News Daily News

Ischemic Cardiomyopathy Patients Can Benefit From Myocardial Unloading, Study Suggests

Michael O'Riordan

October 17, 2016

News Daily News

FDA Warns of Class I Recall for HeartWare VAD Batteries

Michael O'Riordan

June 29, 2016

News Daily News

In-hospital Mortality Higher When IABPs Deployed During PCI

November 04, 2015

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.