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News Daily News

Little Pre- and Postmarket Testing for Most Recalled CV Devices

Michael O'Riordan

September 16, 2024

News Daily News

HeartMate 3 Recalled for Risk of Blood Leaks or Air in System

L.A. McKeown

May 15, 2024

News Daily News

HeartMate II and 3 LVADs Recalled Due to Potential for Outflow Graft Obstruction

Caitlin E. Cox

April 22, 2024

News Daily News

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

Michael O'Riordan

August 10, 2023

News Daily News

Class I Recall for 350,000 Medtronic Defibrillators: FDA

Michael O'Riordan

July 19, 2023

News Daily News

Another Recall Warns of Unheralded Shutdowns With Cardiosave IABPs

Shelley Wood

March 31, 2023

News Daily News

Second Recall in Less Than 2 Months for Cardiosave IABPs

L.A. McKeown

March 17, 2023

News Daily News

FDA: GE Healthcare Recalls Nuclear Medicine Systems Due to Patient Injury Risk

L.A. McKeown

February 16, 2023

News Daily News

Medical Devices Cleared on Faulty Predicates More Likely to be Recalled

Michael O'Riordan

January 17, 2023

News Daily News

FDA: New Fix Available for Medtronic’s Troubled HeartWare VADs

Michael O'Riordan

October 17, 2022

News Daily News

COVID-19: TCTMD’s Dispatch for March Week 3

Todd Neale

March 14, 2022

News Daily News

Penumbra’s JET 7 Recall: A Kick Start to Change?

Caitlin E. Cox

December 01, 2021

News Daily News

Class I Recall for Cordis’ Super Torque Catheters with Radiopaque Markers

Michael O'Riordan

September 23, 2021

News Features

Expired Cardiac Devices May Do Global Good, but Safety Unknown

Yael L. Maxwell

August 26, 2021

News Daily News

Uptick in ‘Implausible’ Cancers Reported After ARB Recalls

L.A. McKeown

August 20, 2021

News Daily News

Critical Limb Ischemia During COVID: Lessons for Care and Clinical Trials

L.A. McKeown

April 26, 2021

News Daily News

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

Michael O'Riordan

February 12, 2021

News Daily News

Lotus Edge TAVR Device Recalled and Discontinued Worldwide

Michael O'Riordan

November 18, 2020

News Opinion Editor's Corner

TCTMD’s Top 10 Most Popular Stories for June 2020

Shelley Wood

July 02, 2020

News Daily News

FDA: Class I Recall for Medtronic’s Pipeline Flex and Pipeline Flex With Shield Technology

Caitlin E. Cox

March 31, 2020

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Little Pre- and Postmarket Testing for Most Recalled CV Devices

HeartMate 3 Recalled for Risk of Blood Leaks or Air in System

HeartMate II and 3 LVADs Recalled Due to Potential for Outflow Graft Obstruction

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

Class I Recall for 350,000 Medtronic Defibrillators: FDA

Another Recall Warns of Unheralded Shutdowns With Cardiosave IABPs

Second Recall in Less Than 2 Months for Cardiosave IABPs

FDA: GE Healthcare Recalls Nuclear Medicine Systems Due to Patient Injury Risk

Medical Devices Cleared on Faulty Predicates More Likely to be Recalled

FDA: New Fix Available for Medtronic’s Troubled HeartWare VADs

COVID-19: TCTMD’s Dispatch for March Week 3

Penumbra’s JET 7 Recall: A Kick Start to Change?

Class I Recall for Cordis’ Super Torque Catheters with Radiopaque Markers

Expired Cardiac Devices May Do Global Good, but Safety Unknown

Uptick in ‘Implausible’ Cancers Reported After ARB Recalls

Critical Limb Ischemia During COVID: Lessons for Care and Clinical Trials

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

Lotus Edge TAVR Device Recalled and Discontinued Worldwide

TCTMD’s Top 10 Most Popular Stories for June 2020

FDA: Class I Recall for Medtronic’s Pipeline Flex and Pipeline Flex With Shield Technology

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