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News Daily News

FDA Warns of Air Embolism Risk With Watchman LAAO Access Systems

Todd Neale

August 06, 2025

News Daily News

Device Correction Issued for HeartMate Monitor Due to Potential Pump Stoppage

Todd Neale

June 28, 2024

News Opinion Off Script

Evoque and Patisiran: A Tale of Two Regulatory Journeys

Sanjay Kaul, MD

March 29, 2024

News Daily News

Asundexian’s Lack of Efficacy Sinks OCEANIC-AF

L.A. McKeown

November 20, 2023

News Daily News

‘Overwhelming Reduction’ in Bleeding With Abelacimab vs Rivaroxaban in AF

L.A. McKeown

September 18, 2023

News Daily News

Class I Recall for Amplatzer LAAO's Steerable Delivery Sheath

Shelley Wood

July 26, 2023

News Daily News

CMS Issues Proposed Coverage Decision to Broaden Access for Carotid Stenting

L.A. McKeown

July 12, 2023

News Daily News

A Simple Nudge Moves the Needle on Statin Prescribing

Michael O'Riordan

December 02, 2022

News Daily News

FDA Investigating Possible Sex Differences in LAAO Outcomes

Todd Neale

September 27, 2021

News Daily News

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

Michael O'Riordan

September 23, 2021

News Daily News

Uptick in ‘Implausible’ Cancers Reported After ARB Recalls

L.A. McKeown

August 20, 2021

News Opinion Editor's Corner

TCTMD’s Top 10 Most Popular Stories for April 2021

Caitlin E. Cox

May 03, 2021

News Daily News

FDA: Class I Recall of Precise PRO Rx Carotid Stent System

Caitlin E. Cox

April 23, 2021

News Daily News

FDA: Penumbra JET 7 Clot Retrievers Recalled Following Deaths, Injuries

Shelley Wood

December 16, 2020

News Daily News

FDA: Class I Recall for Cook Medical’s CrossCath Support Catheters

L.A. McKeown

December 17, 2019

News Daily News

FDA Advisors Recommend CVD Event Reduction Claim for Icosapent Ethyl

Michael O'Riordan

November 14, 2019

News Daily News

FDA: Class I Recall for CentriMag Circulatory Support System Motor

Caitlin E. Cox

November 07, 2019

News Daily News

FDA Expands TAVR Indication to Low-Risk Patients

Michael O'Riordan

August 16, 2019

News Daily News

FDA: Class I Recall for IntraClude Intra-Aortic Occlusion Device

Shelley Wood

July 02, 2019

News Daily News

TCTMD’s Top 10 Most Popular Stories for April 2019

Shelley Wood

May 01, 2019

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FDA Warns of Air Embolism Risk With Watchman LAAO Access Systems

Device Correction Issued for HeartMate Monitor Due to Potential Pump Stoppage

Evoque and Patisiran: A Tale of Two Regulatory Journeys

Asundexian’s Lack of Efficacy Sinks OCEANIC-AF

‘Overwhelming Reduction’ in Bleeding With Abelacimab vs Rivaroxaban in AF

Class I Recall for Amplatzer LAAO's Steerable Delivery Sheath

CMS Issues Proposed Coverage Decision to Broaden Access for Carotid Stenting

A Simple Nudge Moves the Needle on Statin Prescribing

FDA Investigating Possible Sex Differences in LAAO Outcomes

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

Uptick in ‘Implausible’ Cancers Reported After ARB Recalls

TCTMD’s Top 10 Most Popular Stories for April 2021

FDA: Class I Recall of Precise PRO Rx Carotid Stent System

FDA: Penumbra JET 7 Clot Retrievers Recalled Following Deaths, Injuries

FDA: Class I Recall for Cook Medical’s CrossCath Support Catheters

FDA Advisors Recommend CVD Event Reduction Claim for Icosapent Ethyl

FDA: Class I Recall for CentriMag Circulatory Support System Motor

FDA Expands TAVR Indication to Low-Risk Patients

FDA: Class I Recall for IntraClude Intra-Aortic Occlusion Device

TCTMD’s Top 10 Most Popular Stories for April 2019

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