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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

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

Yael L. Maxwell

April 03, 2024

News Daily News

Medtronic Recalls IN.PACT Admiral and IN.PACT AV Catheters

L.A. McKeown

March 31, 2022

News Daily News

Medtronic Recalls TurboHawk Plus Atherectomy System

Todd Neale

March 09, 2022

News Daily News

HawkOne Directional Atherectomy System Recalled Due to Risk of Tip Breakage

L.A. McKeown

January 21, 2022

News Daily News

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

Michael O'Riordan

September 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 Opinion Editor's Corner

TCTMD’s Top 10 Most Popular Stories for September 2017

Shelley Wood

September 30, 2017

News Daily News

FDA: Class I Recall for Venture Catheters

L.A. McKeown

June 21, 2017

News Features

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

Todd Neale

June 21, 2017

News Daily News

Wingman35 Crossing Catheters Recalled Due to Tip Splitting, Separation

Todd Neale

May 04, 2017

News Daily News

Under Surveillance: Ballooning Numbers, Better Survival, Lower-Risk Patients in Latest TVT Registry Data

L.A. McKeown

December 13, 2016

News Daily News

FDA: Global Recall for Roadrunner UniGlide Wire Guides After Coating Contaminated

Michael O'Riordan

August 17, 2016

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FDA Issues Early Alert About Risks of Peripheral Atherectomy Device

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

Medtronic Recalls IN.PACT Admiral and IN.PACT AV Catheters

Medtronic Recalls TurboHawk Plus Atherectomy System

HawkOne Directional Atherectomy System Recalled Due to Risk of Tip Breakage

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

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

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

TCTMD’s Top 10 Most Popular Stories for September 2017

FDA: Class I Recall for Venture Catheters

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

Wingman35 Crossing Catheters Recalled Due to Tip Splitting, Separation

Under Surveillance: Ballooning Numbers, Better Survival, Lower-Risk Patients in Latest TVT Registry Data

FDA: Global Recall for Roadrunner UniGlide Wire Guides After Coating Contaminated

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