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News Daily News

FDA Issues Early Alert About Risks of Peripheral Atherectomy Device

L.A. McKeown

February 07, 2025

News Opinion Editor's Corner

Solutions to TCTMD’s 2024 Cardiology Crossword Challenge

Shelley Wood

January 08, 2025

News Daily News

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

Yael L. Maxwell

April 03, 2024

News Conference News ISET 2024

AI in Pulmonary Embolism: ‘Transformative’ for Patient Care

Caitlin E. Cox

January 30, 2024

News Opinion Editor's Corner

Solutions to TCTMD’s 2023 Cardiology Crossword Challenge

Shelley Wood

January 08, 2024

News Opinion Editor's Corner

TCTMD’s Top 10 Most Popular Stories for July 2023

Shelley Wood

July 31, 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

Medical Devices Cleared on Faulty Predicates More Likely to be Recalled

Michael O'Riordan

January 17, 2023

News Daily News

FDA: Endologix AAA Grafts Get New Labeling That Addresses Endoleak Potential

L.A. McKeown

December 06, 2022

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

FDA Safety Communication Updates Stance on Endologix AAA Grafts

L.A. McKeown

January 13, 2022

News Daily News

Wirion Embolic Protection System Recalled Over Filter Breakage

Todd Neale

January 10, 2022

News Daily News

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

Michael O'Riordan

September 23, 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

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

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FDA Issues Early Alert About Risks of Peripheral Atherectomy Device

Solutions to TCTMD’s 2024 Cardiology Crossword Challenge

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

AI in Pulmonary Embolism: ‘Transformative’ for Patient Care

Solutions to TCTMD’s 2023 Cardiology Crossword Challenge

TCTMD’s Top 10 Most Popular Stories for July 2023

CMS Issues Proposed Coverage Decision to Broaden Access for Carotid Stenting

FDA: All Restrictions on Paclitaxel Devices for PAD Are Removed

Medical Devices Cleared on Faulty Predicates More Likely to be Recalled

FDA: Endologix AAA Grafts Get New Labeling That Addresses Endoleak Potential

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

FDA Safety Communication Updates Stance on Endologix AAA Grafts

Wirion Embolic Protection System Recalled Over Filter Breakage

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

TCTMD’s Top 10 Most Popular Stories for April 2021

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

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