Search - tctmd.com

Displaying 1 - 20 of 36

Sort: Relevancy | Date

FDA Warns of Air Embolism Risk With Watchman LAAO Access Systems

News Daily News

FDA Warns of Air Embolism Risk With Watchman LAAO Access Systems

August 06, 2025

FDA Expresses Continuing Concerns About Getinge/Maquet CV Devices

News Daily News

FDA Expresses Continuing Concerns About Getinge/Maquet CV Devices

May 08, 2024

Class I Recall for 330,000 Radial Artery Catheterization Kits: FDA

News Daily News

Class I Recall for 330,000 Radial Artery Catheterization Kits: FDA

Yael L. Maxwell

April 03, 2024

Evoque and Patisiran: A Tale of Two Regulatory Journeys

News Opinion Off Script

Evoque and Patisiran: A Tale of Two Regulatory Journeys

Sanjay Kaul, MD

March 29, 2024

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

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

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

Medtronic Recalls Parts of Its HeartWare VAD System

News Daily News

Medtronic Recalls Parts of Its HeartWare VAD System

May 29, 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: Class I Recall for Burst Balloons With Sapien 3 Ultra Delivery System

News Daily News

FDA: Class I Recall for Burst Balloons With Sapien 3 Ultra Delivery System

Michael O'Riordan

August 22, 2019

Burst Balloons With Sapien 3 Ultra Prompt ‘Urgent Field Safety Notice’ and Canadian Recall

News Daily News

Burst Balloons With Sapien 3 Ultra Prompt ‘Urgent Field Safety Notice’ and Canadian Recall

July 22, 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

TCTMD’s Top 10 Most Popular Stories for April 2019

News Daily News

TCTMD’s Top 10 Most Popular Stories for April 2019

May 01, 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

Some Stryker Defibrillators Under Recall for ‘Freezing’ Issue

News Daily News

Some Stryker Defibrillators Under Recall for ‘Freezing’ Issue

February 27, 2019

News Opinion Editor's Corner

TCTMD’s Top 10 Most Popular Stories for November 2018

November 30, 2018

SORT-OUT IX: Statistical Mix-up Turns Trial’s Primary Endpoint Around

News Daily News

SORT-OUT IX: Statistical Mix-up Turns Trial’s Primary Endpoint Around

Michael O'Riordan

November 06, 2018

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

Country

First Name

Last Name

Email

Profession

Organization

Country

CAPTCHA

This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.