Search - tctmd.com

Displaying 21 - 40 of 53

Sort: Relevancy | Date

Risk-Based EHR Alert Doesn’t Improve HF Care or Outcomes: REVEAL-HF

News Conference News AHA 2021

Risk-Based EHR Alert Doesn’t Improve HF Care or Outcomes: REVEAL-HF

Michael O'Riordan

November 19, 2021

FDA Investigating Possible Sex Differences in LAAO Outcomes

News Daily News

FDA Investigating Possible Sex Differences in LAAO Outcomes

September 27, 2021

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: Another Class I Recall for HeartWare VAD

News Daily News

FDA: Another Class I Recall for HeartWare VAD

April 16, 2021

FDA: Class I Recall for Seven Models of Medtronic ICDs and CRT-Ds

News Daily News

FDA: Class I Recall for Seven Models of Medtronic ICDs and CRT-Ds

Yael L. Maxwell

April 12, 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

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

Kawasaki Link to COVID-19 in Kids Probed as UK, New York Issue Alerts

News Daily News

Kawasaki Link to COVID-19 in Kids Probed as UK, New York Issue Alerts

May 06, 2020

European Regulators Approve First Transcatheter MV Replacement Device

News Daily News

European Regulators Approve First Transcatheter MV Replacement Device

Michael O'Riordan

January 30, 2020

News Daily News

CV Safety Trial for Lorcaserin Picks Up Cancer Signal: FDA

January 14, 2020

News Daily News

FDA: Some Stryker Defibrillators Require Fix for Failure to Deliver Shock

January 13, 2020

VICTORIA Trial of Vericiguat for Worsening HF Meets Primary Endpoint

News Daily News

VICTORIA Trial of Vericiguat for Worsening HF Meets Primary Endpoint

November 20, 2019

FDA: Class I Recall for CentriMag Circulatory Support System Motor

News Daily News

FDA: Class I Recall for CentriMag Circulatory Support System Motor

November 07, 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

FDA: Class I Recall for Ellipse ICD Due to Faulty Wires

News Daily News

FDA: Class I Recall for Ellipse ICD Due to Faulty Wires

August 05, 2019

FDA Warns of Premature Battery Depletion With Certain Medtronic Pacemakers

News Daily News

FDA Warns of Premature Battery Depletion With Certain Medtronic Pacemakers

Michael O'Riordan

May 07, 2019

FDA Provides Update on Tainted ARB Investigation, With New Impurity Found

News Daily News

FDA Provides Update on Tainted ARB Investigation, With New Impurity Found

March 04, 2019

FDA Warns Healthcare Providers of Potential Rise in Death Rate With Impella RP

News Daily News

FDA Warns Healthcare Providers of Potential Rise in Death Rate With Impella RP

February 04, 2019

News Opinion Editor's Corner

TCTMD’s Top 10 Most Popular Stories for November 2018

November 30, 2018

FDA Warns of Deaths, Stroke With Latest-Generation Total Artificial Heart

News Daily News

FDA Warns of Deaths, Stroke Due to Power System Problems With Total Artificial Heart System

August 17, 2018

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.