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Medline Recalls Valve Pack Kits With Expired Cannulas

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Medline Recalls Valve Pack Kits With Expired Cannulas

Yael L. Maxwell

September 16, 2025

Carotid Wallstent Monorail Recalled Due to Manufacturing Defect

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Carotid Wallstent Monorail Recalled Due to Manufacturing Defect

August 22, 2025

Dimitrios Karmpaliotis, Master Operator and Mentor With ‘Heart of Gold,’ Dies at 53

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Dimitrios Karmpaliotis, Master Operator and Mentor With ‘Heart of Gold,’ Dies at 53

Yael L. Maxwell

June 09, 2025

COMPARE-TAVI 1: Myval Performs Well Against Sapien at 1 Year

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COMPARE-TAVI 1: Myval Performs Well Against Sapien at 1 Year

April 11, 2025

STRIDE: GLP-1 Boosts Walking Capacity in Diabetic PAD Patients

News Daily News ACC 2025

STRIDE: GLP-1 Boosts Walking Capacity in Diabetic PAD Patients

March 29, 2025

Philips Recalls Tack Endovascular Systems and Stops Distribution

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Philips Recalls Tack Endovascular Systems and Stops Distribution

March 03, 2025

Editor’s Pick: TCTMD’s Best Long Reads of 2024

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Editor’s Pick: TCTMD’s Best Long Reads of 2024

December 17, 2024

FDA Issues Safety Communication for Some Accolade Pacemakers

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FDA Issues Safety Communication for Some Accolade Pacemakers

December 16, 2024

Little Pre- and Postmarket Testing for Most Recalled CV Devices

News Daily News

Little Pre- and Postmarket Testing for Most Recalled CV Devices

Michael O'Riordan

September 16, 2024

For Pragmatic RCTs, Patient-Reported ‘Hard’ Events Fall Short

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For Pragmatic RCTs, Patient-Reported ‘Hard’ Events Fall Short

July 25, 2024

FDA Medical Devices Chief Jeff Shuren Announces Retirement

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FDA Medical Devices Chief Jeff Shuren Announces Retirement

July 24, 2024

Device Correction Issued for HeartMate Monitor Due to Potential Pump Stoppage

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Device Correction Issued for HeartMate Monitor Due to Potential Pump Stoppage

June 28, 2024

Hypertension Expert George Bakris Mourned by Colleagues and Friends

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Hypertension Expert George Bakris Mourned by Colleagues and Friends

June 18, 2024

HeartMate 3 Recalled for Risk of Blood Leaks or Air in System

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HeartMate 3 Recalled for Risk of Blood Leaks or Air in System

May 15, 2024

FDA Expresses Continuing Concerns About Getinge/Maquet CV Devices

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FDA Expresses Continuing Concerns About Getinge/Maquet CV Devices

May 08, 2024

HeartMate II and 3 LVADs Recalled Due to Potential for Outflow Graft Obstruction

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HeartMate II and 3 LVADs Recalled Due to Potential for Outflow Graft Obstruction

April 22, 2024

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

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

Yael L. Maxwell

April 03, 2024

DCB in STEMI Match DES Through 5 Years: REVELATION

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DCB in STEMI Match DES Through 5 Years: REVELATION

March 27, 2024

Abiomed Recalls Labeling for Left-Sided Impella Pumps: FDA

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Abiomed Recalls Labeling for Left-Sided Impella Pumps: FDA

March 21, 2024

FDA Scolds Abiomed for Not Seeking a PMA for Its Web-Based User Portal

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FDA Scolds Abiomed for Not Seeking a PMA for Its Web-Based User Portal

October 17, 2023

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