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Displaying 1 - 10 of 10
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Medline Recalls Valve Pack Kits With Expired Cannulas
News Daily News

Medline Recalls Valve Pack Kits With Expired Cannulas

Yael L. Maxwell
Yael L. Maxwell
September 16, 2025
Abbott to Stop Making Trifecta Surgical Aortic Valves
News Daily News

Abbott to Stop Making Trifecta Surgical Aortic Valves

Michael O'Riordan
Michael O'Riordan
July 31, 2023
Abiomed Recalls Certain Impella 5.5 Devices Due to Risk of Purge-Fluid Leaks
News Daily News

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

Caitlin E. Cox
Caitlin E. Cox
June 05, 2023
LivaNova Recalls Some LifeSPARC Controllers Used in Advanced Circulatory Support
News Daily News

LivaNova Recalls Some LifeSPARC Controllers Used in Advanced Circulatory Support

L.A. McKeown
L.A. McKeown
September 30, 2022
Xenotransplant of Pig Heart ‘Just Baby Steps,’ Lead Surgeon Says
News Conference News THT 2022

Xenotransplant of Pig Heart ‘Just Baby Steps,’ Lead Surgeon Says

Yael L. Maxwell
Yael L. Maxwell
February 07, 2022
TCTMD’s Top 10 Most Popular Stories for June 2020
News Opinion Editor's Corner

TCTMD’s Top 10 Most Popular Stories for June 2020

Shelley Wood
Shelley Wood
July 02, 2020
FDA Class I Recall for Boston Scientific’s IMAGER II Angiographic Catheters
News Daily News

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

L.A. McKeown
L.A. McKeown
April 07, 2020
FDA: Class I Recall for CentriMag Circulatory Support System Motor
News Daily News

FDA: Class I Recall for CentriMag Circulatory Support System Motor

Caitlin E. Cox
Caitlin E. Cox
November 07, 2019
FDA: Class I Recall for IntraClude Intra-Aortic Occlusion Device
News Daily News

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

Shelley Wood
Shelley Wood
July 02, 2019
FDA: Class I Recall for Cardiosave Hybrid IABP Due to ‘Fluid Ingress’
News Daily News

FDA: Class I Recall for Cardiosave Hybrid IABP Due to ‘Fluid Ingress’

Caitlin E. Cox
Caitlin E. Cox
June 07, 2018
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