Search - tctmd.com

Displaying 1 - 20 of 40

Sort: Relevancy | Date

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

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 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 Reminder: Yearly, Lifelong Surveillance Needed for Endologix AAA Grafts

L.A. McKeown

December 04, 2020

News Daily News

Paclitaxel DCBs Now Implicated in Death, Amputation in Below-the-Knee CLI

L.A. McKeown

January 15, 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: New Concerns Surface With Endologix Grafts for AAA

L.A. McKeown

October 28, 2019

News Daily News

FDA Warns Against Off-label Use of Wingspan Stent System

Todd Neale

April 25, 2019

Advertisement

FDA Issues Early Alert About Risks of Peripheral Atherectomy Device

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

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

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 Reminder: Yearly, Lifelong Surveillance Needed for Endologix AAA Grafts

Paclitaxel DCBs Now Implicated in Death, Amputation in Below-the-Knee CLI

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

FDA: New Concerns Surface With Endologix Grafts for AAA

FDA Warns Against Off-label Use of Wingspan Stent System

Advertisement

Advertisement

Sign In

Forgot Your Password?

Search TCTMD

CME TITLE

Sign up for our newsletter

Search TCTMD

Submit an Event

Become a PREMIUM MEMBER or LOG IN to view exclusive content

REGISTER for free or LOG IN to view this content