Home/Recalls/CANADA-76947
Health CanadaType II

DLP Antegrade Aortic Root Cardioplegia Cannulae

Published: February 13, 2025Recall ID: 76947Category: generalCountry: Canada

Reason for Recall / Hazard

Performance

Product Description & Identification

DLP Antegrade Aortic Root Cardioplegia Cannulae

Additional Source Details

FieldValue
N I D76947
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/dlp-antegrade-aortic-root-cardioplegia-cannulae
IssuePerformance
TitleDLP Antegrade Aortic Root Cardioplegia Cannulae
ProductDLP Antegrade Aortic Root Cardioplegia Cannulae
Archived0
CategoryCardiovascular
Last updated2025-02-13
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert