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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

The More Tweaks Made to PMA-Approved Devices, the More Likely a Recall

News Daily News

The More Tweaks Made to PMA-Approved Devices, the More Likely a Recall

April 13, 2023

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

News Daily News

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

Michael O'Riordan

October 17, 2022

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

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

December 01, 2021

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

News Daily News

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

Michael O'Riordan

September 23, 2021

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

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

Michael O'Riordan

February 12, 2021

FDA Class I Recall for PTA Catheters Due to Unexpected Balloon Bursting

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FDA Class I Recall for PTA Catheters Due to Unexpected Balloon Bursting

Yael L. Maxwell

June 18, 2019

Global Investigative Journalism Initiative Takes Aim at Medical Device Industry

News Daily News

Global Investigative Journalism Initiative Takes Aim at Medical Device Industry

November 26, 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

April 20, 2018

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