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Medline Recalls Valve Pack Kits With Expired Cannulas

Yael L. Maxwell

September 16, 2025

News Daily News

Abiomed Recalls Certain Impella 5.5 Devices Due to Risk of Purge-Fluid Leaks

Caitlin E. Cox

June 05, 2023

News Daily News

FDA Alert: Possible Early Deterioration of Abbott Trifecta SAVR Valves

Todd Neale

February 27, 2023

News Daily News

LivaNova Recalls Some LifeSPARC Controllers Used in Advanced Circulatory Support

L.A. McKeown

September 30, 2022

News Daily News

FDA Safety Communication Updates Stance on Endologix AAA Grafts

L.A. McKeown

January 13, 2022

News Daily News

CMS Releases Proposed Updates for Coverage of Transcatheter MV Repair

Todd Neale

July 01, 2020

News Daily News

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

L.A. McKeown

April 07, 2020

News Daily News

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

Shelley Wood

February 24, 2020

News Daily News

FDA: Class I Recall for CentriMag Circulatory Support System Motor

Caitlin E. Cox

November 07, 2019

News Daily News

FDA Expands TAVR Indication to Low-Risk Patients

Michael O'Riordan

August 16, 2019

News Daily News

FDA: Class I Recall for IntraClude Intra-Aortic Occlusion Device

Shelley Wood

July 02, 2019

News Daily News

TCTMD’s Top 10 Most Popular Stories for April 2019

Shelley Wood

May 01, 2019

News Daily News

FDA Recommends Caution When Using Heater-Cooler Devices in Cardiothoracic Surgery

L.A. McKeown

October 14, 2016

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Medline Recalls Valve Pack Kits With Expired Cannulas

Abiomed Recalls Certain Impella 5.5 Devices Due to Risk of Purge-Fluid Leaks

FDA Alert: Possible Early Deterioration of Abbott Trifecta SAVR Valves

LivaNova Recalls Some LifeSPARC Controllers Used in Advanced Circulatory Support

FDA Safety Communication Updates Stance on Endologix AAA Grafts

CMS Releases Proposed Updates for Coverage of Transcatheter MV Repair

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

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

FDA: Class I Recall for CentriMag Circulatory Support System Motor

FDA Expands TAVR Indication to Low-Risk Patients

FDA: Class I Recall for IntraClude Intra-Aortic Occlusion Device

TCTMD’s Top 10 Most Popular Stories for April 2019

FDA Recommends Caution When Using Heater-Cooler Devices in Cardiothoracic Surgery

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