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Andexanet Alfa Pulled From US Market

Todd Neale

December 22, 2025

News Daily News

FDA: All Restrictions on Paclitaxel Devices for PAD Are Removed

L.A. McKeown

July 11, 2023

News Daily News

Uptick in ‘Implausible’ Cancers Reported After ARB Recalls

L.A. McKeown

August 20, 2021

News Daily News

Medtronic Recalls Valiant Navion TEVAR Stent Grafts

Shelley Wood

February 17, 2021

News Daily News

CV Safety Trial for Lorcaserin Picks Up Cancer Signal: FDA

Shelley Wood

January 14, 2020

News Daily News

FDA Advisors Recommend CVD Event Reduction Claim for Icosapent Ethyl

Michael O'Riordan

November 14, 2019

News Daily News

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

Shelley Wood

July 22, 2019

News Daily News

FDA Tallies Cases of Fournier Gangrene in Patients Taking SGLT2 Inhibitors

Michael O'Riordan

May 08, 2019

News Opinion Editor's Corner

TCTMD’s Top 10 Most Popular Stories for January 2019

Caitlin E. Cox

January 31, 2019

News Conference News ISET 2019

Paclitaxel in PAD: What to Tell Patients While the Numbers Are Crunched

Caitlin E. Cox

January 28, 2019

News Opinion Editor's Corner

TCTMD’s Top 10 Most Popular Stories for November 2018

Shelley Wood

November 30, 2018

News Daily News

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

Michael O'Riordan

November 06, 2018

News Daily News

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

L.A. McKeown

October 16, 2018

News Opinion Editor's Corner

TCTMD’s Top 10 Most Popular Stories for August 2018

Caitlin E. Cox

September 04, 2018

News Daily News

Abciximab in ‘Short Supply’ Worldwide

Shelley Wood

April 13, 2018

News Daily News

Manufacturing Defect Leads to Recall of Implanted Medtronic CRT-D Devices, ICDs

Todd Neale

February 27, 2018

News Daily News

Edwards Voluntarily Recalls Cardioband ‘Anchors’ Used in Mitral and Tricuspid Repair

Michael O'Riordan

February 27, 2018

News Daily News

Absorb BVS Use Restricted in Europe

Michael O'Riordan

April 06, 2017

News Daily News

Boston Scientific Recalls All Lotus Valves, Including Lotus With Depth Guard

Michael O'Riordan

February 23, 2017

News Daily News

Boston Scientific Announces Fix for Lotus Edge TAVR Device Following Implantation ‘Pause’

L.A. McKeown

January 11, 2017

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Andexanet Alfa Pulled From US Market

FDA: All Restrictions on Paclitaxel Devices for PAD Are Removed

Uptick in ‘Implausible’ Cancers Reported After ARB Recalls

Medtronic Recalls Valiant Navion TEVAR Stent Grafts

CV Safety Trial for Lorcaserin Picks Up Cancer Signal: FDA

FDA Advisors Recommend CVD Event Reduction Claim for Icosapent Ethyl

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

FDA Tallies Cases of Fournier Gangrene in Patients Taking SGLT2 Inhibitors

TCTMD’s Top 10 Most Popular Stories for January 2019

Paclitaxel in PAD: What to Tell Patients While the Numbers Are Crunched

TCTMD’s Top 10 Most Popular Stories for November 2018

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

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

TCTMD’s Top 10 Most Popular Stories for August 2018

Abciximab in ‘Short Supply’ Worldwide

Manufacturing Defect Leads to Recall of Implanted Medtronic CRT-D Devices, ICDs

Edwards Voluntarily Recalls Cardioband ‘Anchors’ Used in Mitral and Tricuspid Repair

Absorb BVS Use Restricted in Europe

Boston Scientific Recalls All Lotus Valves, Including Lotus With Depth Guard

Boston Scientific Announces Fix for Lotus Edge TAVR Device Following Implantation ‘Pause’

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