Home/Recalls/CANADA-59331
Health CanadaType II

HeartMate 3 Sealed Outflow Graft with bend relief (2019-03-31)

Published: April 12, 2019Recall ID: 59331Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

HeartMate 3 Sealed Outflow Graft with bend relief (2019-03-31)

Additional Source Details

FieldValue
N I D59331
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/heartmate-3-sealed-outflow-graft-bend-relief-2019-03-31
IssueMedical devices
Title HeartMate 3 Sealed Outflow Graft with bend relief (2019-03-31)
Archived0
CategoryMedical devices
Last updated2019-04-12
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert