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Displaying 101 - 120 of 155
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TCTMD’s Top 10 Most Popular Stories for August 2018
News Opinion Editor's Corner

TCTMD’s Top 10 Most Popular Stories for August 2018

Caitlin E. Cox
Caitlin E. Cox
September 04, 2018
High-Risk Medical Device Approval Process in Europe Inches Towards Transparency
News Daily News

High-Risk Medical Device Approval Process in Europe Inches Towards Transparency

Michael O'Riordan
Michael O'Riordan
July 20, 2018
FDA Recalls Valsartan-Containing Drugs After Detection of Carcinogen
News Daily News

FDA Recalls Valsartan-Containing Drugs After Detection of Carcinogen

Michael O'Riordan
Michael O'Riordan
July 16, 2018
USPSTF: Insufficient Evidence to Support CAC Score, hsCRP, or ABI for Risk Assessment
News Daily News

USPSTF: Insufficient Evidence to Support CAC Score, hsCRP, or ABI for Risk Assessment

Michael O'Riordan
Michael O'Riordan
July 12, 2018
Jack V. Tu, Tireless Cardiovascular Researcher and Mentor, Dies at 53
News Daily News

Jack V. Tu, Tireless Cardiovascular Researcher and Mentor, Dies at 53

L.A. McKeown
L.A. McKeown
June 07, 2018
FDA: Class I Recall for Cardiosave Hybrid IABP Due to ‘Fluid Ingress’
News Daily News

FDA: Class I Recall for Cardiosave Hybrid IABP Due to ‘Fluid Ingress’

Caitlin E. Cox
Caitlin E. Cox
June 07, 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
Michael O'Riordan
June 04, 2018
News Industry News

FDA Classifies HeartWare(TM) HVAD(TM) Systems Unexpected Power Source Switching as Class I Recall

June 04, 2018
News Daily News

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

Todd Neale
Todd Neale
May 23, 2018
FDA’s ‘Medical Device Safety Action Plan’ Focuses on Product Life Cycles and Preventing Cyberattacks
News Daily News

FDA’s ‘Medical Device Safety Action Plan’ Focuses on Product Life Cycles and Preventing Cyberattacks

L.A. McKeown
L.A. McKeown
April 20, 2018
Manufacturing Defect Leads to Recall of Implanted Medtronic CRT-D Devices, ICDs
News Daily News

Manufacturing Defect Leads to Recall of Implanted Medtronic CRT-D Devices, ICDs

Todd Neale
Todd Neale
February 27, 2018
#CardiologyToo? Sexual Harassment Also Infects Hospital Corridors and the Cath Lab
News Features

#CardiologyToo? Sexual Harassment Also Infects Hospital Corridors and the Cath Lab

Yael L. Maxwell
Yael L. Maxwell
January 19, 2018
IABPs Recalled Due to False Blood Detection Alarms and Ingress of Fluid
News Daily News

IABPs Recalled Due to False Blood Detection Alarms and Ingress of Fluid

L.A. McKeown
L.A. McKeown
September 06, 2017
FDA: Class I Recall for Cook’s Thoracic Endovascular Grafts
News Daily News

FDA: Class I Recall for Cook’s Thoracic Endovascular Grafts

Michael O'Riordan
Michael O'Riordan
August 17, 2017
News Daily News

FDA Deems ‘Field Action’ for Faulty IABPs a Class I Recall

Shelley Wood
Shelley Wood
August 07, 2017
Penumbra Stent Retriever Recalled Due to Potential for Wire to Break, Separate
News Daily News

Penumbra Stent Retriever Recalled Due to Potential for Wire to Break, Separate

Todd Neale
Todd Neale
July 21, 2017
News Daily News

FDA: Class I Recall for Venture Catheters

L.A. McKeown
L.A. McKeown
June 21, 2017
Reacting to REPRISE III: Enthusiasm, Explanations, and Caveats for the Lotus Pivotal TAVR Trial
News Conference News TVT 2017

Reacting to REPRISE III: Enthusiasm, Explanations, and Caveats for the Lotus Pivotal TAVR Trial

Shelley Wood
Shelley Wood
June 16, 2017
News Daily News

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

Todd Neale
Todd Neale
May 24, 2017
News Daily News

Abbott Vascular Recalls Three Coronary Catheters Because of Possible Sheath Removal Problems

Todd Neale
Todd Neale
May 16, 2017

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