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Little Pre- and Postmarket Testing for Most Recalled CV Devices

News Daily News

Little Pre- and Postmarket Testing for Most Recalled CV Devices

Michael O'Riordan

September 16, 2024

TCTMD’s Top 10 Most Popular Stories for March 2024

News Opinion Editor's Corner

TCTMD’s Top 10 Most Popular Stories for March 2024

April 03, 2024

TCTMD’s Top 10 Most Popular Stories for July 2023

News Opinion Editor's Corner

TCTMD’s Top 10 Most Popular Stories for July 2023

July 31, 2023

Class I Recall for 350,000 Medtronic Defibrillators: FDA

News Daily News

Class I Recall for 350,000 Medtronic Defibrillators: FDA

Michael O'Riordan

July 19, 2023

TCTMD’s Top 10 Most Popular Stories for June 2023

News Opinion Editor's Corner

TCTMD’s Top 10 Most Popular Stories for June 2023

July 03, 2023

Medical Devices Cleared on Faulty Predicates More Likely to be Recalled

News Daily News

Medical Devices Cleared on Faulty Predicates More Likely to be Recalled

Michael O'Riordan

January 17, 2023

Class I Recall for Boston Scientific Ingenio Pacemaker and CRT Devices

News Daily News

Class I Recall for Boston Scientific Ingenio Pacemaker and CRT Devices

August 09, 2021

TCTMD’s Top 10 Most Popular Stories for April 2021

News Opinion Editor's Corner

TCTMD’s Top 10 Most Popular Stories for April 2021

May 03, 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 Issues Class I Recall for Emblem S-ICD Over Electrode Fractures

News Daily News

FDA Issues Class I Recall for Emblem S-ICD Over Electrode Fractures

Michael O'Riordan

February 12, 2021

News Daily News

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

January 13, 2020

Safe to Leave Recalled Sprint Fidelis ICD Leads in Place? Debate Continues

News Daily News

Safe to Leave Recalled Sprint Fidelis ICD Leads in Place? Debate Continues

August 28, 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

Some Stryker Defibrillators Under Recall for ‘Freezing’ Issue

News Daily News

Some Stryker Defibrillators Under Recall for ‘Freezing’ Issue

February 27, 2019

Class I Recall for Certain Medtronic Pacemakers Due to Possible Circuit Error

News Daily News

Class I Recall for Certain Medtronic Pacemakers Due to Possible Circuit Error

February 15, 2019

More INR Test Strips Recalled Due to Inaccurately High Results

News Daily News

More INR Test Strips Recalled Due to Inaccurately High Results

December 21, 2018

INR Test Strips Recalled Due to Inaccurate Measurements

News Daily News

INR Test Strips Recalled Due to Inaccurate Measurements

November 02, 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

February 27, 2018

News Daily News

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

March 24, 2017

News Daily News

Recall Underway for AED Electrodes With Compatibility Problems

October 17, 2016

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