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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

Abiomed Recalls Labeling for Left-Sided Impella Pumps: FDA

Caitlin E. Cox

March 21, 2024

News Daily News

FDA: All Restrictions on Paclitaxel Devices for PAD Are Removed

L.A. McKeown

July 11, 2023

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: Medtronic Stops Production and Distribution of Troubled HeartWare VAD

L.A. McKeown

June 03, 2021

News Daily News

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

L.A. McKeown

December 17, 2019

News Daily News

FDA Class I Recall for PTA Catheters Due to Unexpected Balloon Bursting

Yael L. Maxwell

June 18, 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: Class I Recall for Venture Catheters

L.A. McKeown

June 21, 2017

News Daily News

Wingman35 Crossing Catheters Recalled Due to Tip Splitting, Separation

Todd Neale

May 04, 2017

News Daily News

FDA Announces Recall of Bard’s Halo One Peripheral Vascular Guiding Sheath

L.A. McKeown

January 31, 2017

News Daily News

FDA: Vascu-Guard Patch Associated With Bleeding, Death After Carotid Endarterectomy

Yael L. Maxwell

September 02, 2016

News Daily News

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

Michael O'Riordan

August 17, 2016

News Daily News

Cook Medical Issues Recall for Beacon Tip Catheters

Shelley Wood

May 04, 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

Abiomed Recalls Labeling for Left-Sided Impella Pumps: FDA

FDA: All Restrictions on Paclitaxel Devices for PAD Are Removed

Medtronic Recalls TurboHawk Plus Atherectomy System

HawkOne Directional Atherectomy System Recalled Due to Risk of Tip Breakage

FDA: Medtronic Stops Production and Distribution of Troubled HeartWare VAD

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

FDA Class I Recall for PTA Catheters Due to Unexpected Balloon Bursting

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

FDA: Class I Recall for Venture Catheters

Wingman35 Crossing Catheters Recalled Due to Tip Splitting, Separation

FDA Announces Recall of Bard’s Halo One Peripheral Vascular Guiding Sheath

FDA: Vascu-Guard Patch Associated With Bleeding, Death After Carotid Endarterectomy

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

Cook Medical Issues Recall for Beacon Tip Catheters

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