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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

FDA: Class I Recall of Cobalt and Crome ICDs and CRT-Ds Due to Reduced-Energy Shock

News Daily News

FDA: Class I Recall of Cobalt and Crome ICDs and CRT-Ds Due to Reduced-Energy Shock

August 19, 2022

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

News Daily News

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

January 13, 2020

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 Warns of Cybersecurity Vulnerabilities With Some Medtronic Implanted Devices

News Daily News

FDA Warns of Cybersecurity Vulnerabilities With Some Medtronic Implanted Devices

Michael O'Riordan

March 22, 2019

Some Stryker Defibrillators Under Recall for ‘Freezing’ Issue

News Daily News

Some Stryker Defibrillators Under Recall for ‘Freezing’ Issue

February 27, 2019

FDA Touts Increased Oversight of Medical Device Makers

News Daily News

FDA Touts Increased Oversight of Medical Device Makers

Michael O'Riordan

November 22, 2018

FDA: Battery, Cybersecurity Issues With ICDs and CRT-Ds Now Have Firmware Fix

News Daily News

FDA: Battery, Cybersecurity Issues With ICDs and CRT-Ds Now Have Firmware Fix

April 17, 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

FDA Warns Certain Zoll LifeVests Might Fail to Deliver Shocks

News Daily News

FDA Warns Certain Zoll LifeVests Might Fail to Deliver Shocks

Michael O'Riordan

January 17, 2018

News Daily News

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

March 24, 2017

News Daily News

FDA Warns of Cybersecurity Holes in Certain Cardiac Devices and Monitoring System

Yael L. Maxwell

January 09, 2017

News Daily News

Recall Underway for AED Electrodes With Compatibility Problems

October 17, 2016

News Daily News

St. Jude Medical Warns of Rapid, Unexpected, and Potentially Lethal Battery Depletions With ICDs, CRT-Ds

October 11, 2016

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