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News Daily News

FDA Issues Early Alert About Risks of Peripheral Atherectomy Device

L.A. McKeown

February 07, 2025

News Daily News

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

Caitlin E. Cox

July 27, 2023

News Daily News

CMS Issues Proposed Coverage Decision to Broaden Access for Carotid Stenting

L.A. McKeown

July 12, 2023

News Daily News

FDA: All Restrictions on Paclitaxel Devices for PAD Are Removed

L.A. McKeown

July 11, 2023

News Daily News

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

Michael O'Riordan

September 23, 2021

News Daily News

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

Caitlin E. Cox

April 23, 2021

News Daily News

Medtronic Recalls Valiant Navion TEVAR Stent Grafts

Shelley Wood

February 17, 2021

News Daily News

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

Shelley Wood

December 16, 2020

News Daily News

FDA Warns of Potential Medical Device Shortage Due to Sterilization Woes

Yael L. Maxwell

October 25, 2019

News Daily News

TCTMD’s Top 10 Most Popular Stories for April 2019

Shelley Wood

May 01, 2019

News Daily News

FDA Warns Against Off-label Use of Wingspan Stent System

Todd Neale

April 25, 2019

News Daily News

FDA Analysis Points to Higher Death Risk With Paclitaxel-Based Devices for PAD

L.A. McKeown

March 15, 2019

News Daily News

Mortality Data ‘Inadvertently Omitted’ From IN.PACT Analysis of Paclitaxel-Coated Balloons

L.A. McKeown

February 19, 2019

News Daily News

FDA Alerts Doctors to Potential Late Risks With Paclitaxel-Coated Balloons and Stents in PAD

Michael O'Riordan

January 17, 2019

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 Identifies Culprit in Endovascular Graft Type III Endoleaks

L.A. McKeown

June 19, 2018

News Daily News

No More Absorb BVS: Abbott Puts a Stop to Sales

Caitlin E. Cox

September 08, 2017

News Daily News

Penumbra Stent Retriever Recalled Due to Potential for Wire to Break, Separate

Todd Neale

July 21, 2017

News Daily News

Absorb BVS Recalled in Australia From All Centers Not Studying Device

Shelley Wood

May 03, 2017

News Daily News

TCTMD’s Top 10 Most Popular Stories for April 2017

Shelley Wood

April 28, 2017

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FDA Issues Early Alert About Risks of Peripheral Atherectomy Device

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

CMS Issues Proposed Coverage Decision to Broaden Access for Carotid Stenting

FDA: All Restrictions on Paclitaxel Devices for PAD Are Removed

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

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

Medtronic Recalls Valiant Navion TEVAR Stent Grafts

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

FDA Warns of Potential Medical Device Shortage Due to Sterilization Woes

TCTMD’s Top 10 Most Popular Stories for April 2019

FDA Warns Against Off-label Use of Wingspan Stent System

FDA Analysis Points to Higher Death Risk With Paclitaxel-Based Devices for PAD

Mortality Data ‘Inadvertently Omitted’ From IN.PACT Analysis of Paclitaxel-Coated Balloons

FDA Alerts Doctors to Potential Late Risks With Paclitaxel-Coated Balloons and Stents in PAD

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

FDA Identifies Culprit in Endovascular Graft Type III Endoleaks

No More Absorb BVS: Abbott Puts a Stop to Sales

Penumbra Stent Retriever Recalled Due to Potential for Wire to Break, Separate

Absorb BVS Recalled in Australia From All Centers Not Studying Device

TCTMD’s Top 10 Most Popular Stories for April 2017

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