Home/Recalls/CANADA-82009
Health CanadaType II

Medtronic DLP Retrograde Cardioplegia Cannulae

Published: April 30, 2026Recall ID: 82009Category: generalCountry: Canada

Reason for Recall / Hazard

Sterility

Product Description & Identification

Medtronic DLP Retrograde Cardioplegia Cannulae

Additional Source Details

FieldValue
N I D82009
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/medtronic-dlp-retrograde-cardioplegia-cannulae
IssueSterility
TitleMedtronic DLP Retrograde Cardioplegia Cannulae
ProductMedtronic DLP Retrograde Cardioplegia Cannulae
Archived0
CategoryCardiovascular
Last updated2026-04-30
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert