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News Daily News

Device Correction Issued for HeartMate Monitor Due to Potential Pump Stoppage

Todd Neale

June 28, 2024

News Daily News

FDA Scolds Abiomed for Not Seeking a PMA for Its Web-Based User Portal

Caitlin E. Cox

October 17, 2023

News Daily News

Cardiosave IABPs Recalled Again, This Time Due to Potential Electrical Problems: FDA

Michael O'Riordan

August 10, 2023

News Daily News

FDA: Class I Recall for Left-Sided Impella Pumps Due to TAVI Interaction

Caitlin E. Cox

July 27, 2023

News Daily News

Another Recall Warns of Unheralded Shutdowns With Cardiosave IABPs

Shelley Wood

March 31, 2023

News Daily News

New IABP Recall: Balloon Catheter Damage Might Cause Bleeding Into Pump

Shelley Wood

January 25, 2023

News Daily News

FDA: Another Class I Recall for HeartWare VAD

Shelley Wood

April 16, 2021

News Daily News

FDA: Class I Recall for HeartWare VAD Pump Implant Kit

Shelley Wood

March 01, 2021

News Daily News

Medtronic Recalls Parts of Its HeartWare VAD System

Todd Neale

May 29, 2020

News Daily News

FDA: Class I Recall for CentriMag Circulatory Support System Motor

Caitlin E. Cox

November 07, 2019

News Daily News

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

Shelley Wood

August 05, 2019

News Daily News

FDA Warns of Premature Battery Depletion With Certain Medtronic Pacemakers

Michael O'Riordan

May 07, 2019

News Daily News

Two Pediatric Cardiac Catheters Recalled for Defective Balloons

L.A. McKeown

April 26, 2019

News Opinion Editor's Corner

TCTMD’s Top 10 Most Popular Stories for September 2017

Shelley Wood

September 30, 2017

News Opinion Editor's Corner

TCTMD’s Top 10 Most Popular Stories for May 2017

Shelley Wood

June 01, 2017

News Daily News

FDA: Class I Recall for Over 47,000 HeartStart MRx Monitor/Defibrillator Units

L.A. McKeown

March 24, 2017

News Daily News

Medtronic Warns of Vascular Trauma, Some Resulting in Death, With CoreValve’s EnVeo R Delivery Catheter

Michael O'Riordan

August 18, 2016

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Device Correction Issued for HeartMate Monitor Due to Potential Pump Stoppage

FDA Scolds Abiomed for Not Seeking a PMA for Its Web-Based User Portal

Cardiosave IABPs Recalled Again, This Time Due to Potential Electrical Problems: FDA

FDA: Class I Recall for Left-Sided Impella Pumps Due to TAVI Interaction

Another Recall Warns of Unheralded Shutdowns With Cardiosave IABPs

New IABP Recall: Balloon Catheter Damage Might Cause Bleeding Into Pump

FDA: Another Class I Recall for HeartWare VAD

FDA: Class I Recall for HeartWare VAD Pump Implant Kit

Medtronic Recalls Parts of Its HeartWare VAD System

FDA: Class I Recall for CentriMag Circulatory Support System Motor

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

FDA Warns of Premature Battery Depletion With Certain Medtronic Pacemakers

Two Pediatric Cardiac Catheters Recalled for Defective Balloons

TCTMD’s Top 10 Most Popular Stories for September 2017

TCTMD’s Top 10 Most Popular Stories for May 2017

FDA: Class I Recall for Over 47,000 HeartStart MRx Monitor/Defibrillator Units

Medtronic Warns of Vascular Trauma, Some Resulting in Death, With CoreValve’s EnVeo R Delivery Catheter

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