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Andexanet Alfa Pulled From US Market

News Daily News

Andexanet Alfa Pulled From US Market

December 22, 2025

FDA Issues Safety Communication for Some Accolade Pacemakers

News Daily News

FDA Issues Safety Communication for Some Accolade Pacemakers

December 16, 2024

FDA: No Signs of Link Between GLP-1s and Suicidal Thoughts, Actions

News Daily News

FDA: No Signs of Link Between GLP-1s and Suicidal Thoughts, Actions

January 12, 2024

FDA: Endologix AAA Grafts Get New Labeling That Addresses Endoleak Potential

News Daily News

FDA: Endologix AAA Grafts Get New Labeling That Addresses Endoleak Potential

December 06, 2022

FDA Safety Communication Updates Stance on Endologix AAA Grafts

News Daily News

FDA Safety Communication Updates Stance on Endologix AAA Grafts

January 13, 2022

FDA Reminder: Yearly, Lifelong Surveillance Needed for Endologix AAA Grafts

News Daily News

FDA Reminder: Yearly, Lifelong Surveillance Needed for Endologix AAA Grafts

December 04, 2020

Hydroxychloroquine: No Help, Clear Harm in COVID-19 RCT and Cohort Studies

News Features

Hydroxychloroquine: No Help, Clear Harm in COVID-19 RCT and Cohort Studies

May 20, 2020

FDA: New Concerns Surface With Endologix Grafts for AAA

News Daily News

FDA: New Concerns Surface With Endologix Grafts for AAA

October 28, 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 Against Off-label Use of Wingspan Stent System

News Daily News

FDA Warns Against Off-label Use of Wingspan Stent System

April 25, 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

FDA: All AFX Endovascular AAA Systems Now Under Class I Recall

News Daily News

FDA: All AFX Endovascular AAA Systems Now Under Class I Recall

October 16, 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

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

FDA: Clarithromycin Risks Persist in Patients With CAD

News Daily News

FDA: Clarithromycin Risks Persist in Patients With CAD

February 26, 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

Inferior Vena Cava Filter Use Fell After FDA Warning but Remains High

News Daily News

Inferior Vena Cava Filter Use Fell After FDA Warning but Remains High

July 12, 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

FDA Classifies Latest HeartWare VAD Recalls as Class I

Michael O'Riordan

October 24, 2016

News Daily News

FDA Recommends Caution When Using Heater-Cooler Devices in Cardiothoracic Surgery

October 14, 2016

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