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

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

March 31, 2022

Medtronic Recalls TurboHawk Plus Atherectomy System

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Medtronic Recalls TurboHawk Plus Atherectomy System

March 09, 2022

HawkOne Directional Atherectomy System Recalled Due to Risk of Tip Breakage

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HawkOne Directional Atherectomy System Recalled Due to Risk of Tip Breakage

January 21, 2022

FDA Safety Communication Updates Stance on Endologix AAA Grafts

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FDA Safety Communication Updates Stance on Endologix AAA Grafts

January 13, 2022

Wirion Embolic Protection System Recalled Over Filter Breakage

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Wirion Embolic Protection System Recalled Over Filter Breakage

January 10, 2022

Class I Recall of Batteries for Cardiosave Hybrid/Rescue IABPs: FDA

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Class I Recall of Batteries for Cardiosave Hybrid/Rescue IABPs: FDA

October 29, 2021

FDA Investigating Possible Sex Differences in LAAO Outcomes

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FDA Investigating Possible Sex Differences in LAAO Outcomes

September 27, 2021

Medtronic Vascular Recalls Angiographic Guidewire Components

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Medtronic Vascular Recalls Angiographic Guidewire Components

July 02, 2021

Papers Probe Temporal Link Between COVID-19 Vaccines and Myocarditis

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Papers Probe Temporal Link Between COVID-19 Vaccines and Myocarditis

Michael O'Riordan

June 17, 2021

TCTMD’s Top 10 Most Popular Stories for April 2021

News Opinion Editor's Corner

TCTMD’s Top 10 Most Popular Stories for April 2021

May 03, 2021

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

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

April 23, 2021

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

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

December 16, 2020

FDA Reminder: Yearly, Lifelong Surveillance Needed for Endologix AAA Grafts

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FDA Reminder: Yearly, Lifelong Surveillance Needed for Endologix AAA Grafts

December 04, 2020

Lotus Edge TAVR Device Recalled and Discontinued Worldwide

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Lotus Edge TAVR Device Recalled and Discontinued Worldwide

Michael O'Riordan

November 18, 2020

CMS Releases Proposed Updates for Coverage of Transcatheter MV Repair

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CMS Releases Proposed Updates for Coverage of Transcatheter MV Repair

July 01, 2020

FDA: Class I Recall for Vascular Solutions’ Dual Lumen Catheters

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FDA: Class I Recall for Vascular Solutions’ Dual Lumen Catheters

May 01, 2020

FDA Class I Recall for Boston Scientific’s IMAGER II Angiographic Catheters

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FDA Class I Recall for Boston Scientific’s IMAGER II Angiographic Catheters

April 07, 2020

FDA: Abbott Recalls NC Trek RX and NC Traveler Coronary Catheters

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FDA: Abbott Recalls NC Trek RX and NC Traveler Coronary Catheters

February 24, 2020

FDA: New Concerns Surface With Endologix Grafts for AAA

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FDA: New Concerns Surface With Endologix Grafts for AAA

October 28, 2019

FDA: Class I Recall for Medtronic’s 6-Fr Sherpa NX Guide Catheter

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FDA: Class I Recall for Medtronic’s 6-Fr Sherpa NX Guide Catheter

Michael O'Riordan

October 09, 2019

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