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Displaying 1 - 20 of 21
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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

Todd Neale
Todd Neale
August 06, 2025
DETECT-AS: Alert System Increases AV Replacement in Eligible Patients
News Conference News ACC 2025

DETECT-AS: Alert System Increases AV Replacement in Eligible Patients

Michael O'Riordan
Michael O'Riordan
April 04, 2025
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
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
Sanjay Kaul, MD
March 29, 2024
FDA: Class I Recall for Left-Sided Impella Pumps Due to TAVI Interaction
News Daily News

FDA: Class I Recall for Left-Sided Impella Pumps Due to TAVI Interaction

Caitlin E. Cox
Caitlin E. Cox
July 27, 2023
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
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

L.A. McKeown
L.A. McKeown
December 06, 2022
FDA Safety Communication Updates Stance on Endologix AAA Grafts
News Daily News

FDA Safety Communication Updates Stance on Endologix AAA Grafts

L.A. McKeown
L.A. McKeown
January 13, 2022
Papers Probe Temporal Link Between COVID-19 Vaccines and Myocarditis
News Daily News

Papers Probe Temporal Link Between COVID-19 Vaccines and Myocarditis

Michael O'Riordan
Michael O'Riordan
June 17, 2021
FDA Reminder: Yearly, Lifelong Surveillance Needed for Endologix AAA Grafts
News Daily News

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

L.A. McKeown
L.A. McKeown
December 04, 2020
Lotus Edge TAVR Device Recalled and Discontinued Worldwide
News Daily News

Lotus Edge TAVR Device Recalled and Discontinued Worldwide

Michael O'Riordan
Michael O'Riordan
November 18, 2020
FDA: Abbott Recalls NC Trek RX and NC Traveler Coronary Catheters
News Daily News

FDA: Abbott Recalls NC Trek RX and NC Traveler Coronary Catheters

Shelley Wood
Shelley Wood
February 24, 2020
FDA: New Concerns Surface With Endologix Grafts for AAA
News Daily News

FDA: New Concerns Surface With Endologix Grafts for AAA

L.A. McKeown
L.A. McKeown
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
Michael O'Riordan
August 22, 2019
TCTMD’s Top 10 Most Popular Stories for April 2019
News Daily News

TCTMD’s Top 10 Most Popular Stories for April 2019

Shelley Wood
Shelley Wood
May 01, 2019
Some Stryker Defibrillators Under Recall for ‘Freezing’ Issue
News Daily News

Some Stryker Defibrillators Under Recall for ‘Freezing’ Issue

Todd Neale
Todd Neale
February 27, 2019
TCTMD’s Top 10 Most Popular Stories for January 2019
News Opinion Editor's Corner

TCTMD’s Top 10 Most Popular Stories for January 2019

Caitlin E. Cox
Caitlin E. Cox
January 31, 2019
News Opinion Editor's Corner

TCTMD’s Top 10 Most Popular Stories for November 2018

Shelley Wood
Shelley Wood
November 30, 2018
Catheter Kerfuffle: How Concerning Is Off-Label Use in Stroke Interventions?
News Features

Catheter Kerfuffle: How Concerning Is Off-Label Use in Stroke Interventions?

Todd Neale
Todd Neale
June 21, 2017
Absorb in Europe: When, How, and by Whom the Beleaguered BVS Is Being Used After Restrictions
News Features

Absorb in Europe: When, How, and by Whom the Beleaguered BVS Is Being Used After Restrictions

Michael O'Riordan
Michael O'Riordan
May 08, 2017

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