Home/Recalls/CANADA-48061
Health CanadaType II

Angiojet Ultra 5000a Console (2019-11-11)

Published: December 13, 2019Recall ID: 48061Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

Angiojet Ultra 5000a Console (2019-11-11)

Additional Source Details

FieldValue
N I D48061
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/angiojet-ultra-5000a-console-2019-11-11
IssueMedical devices
Title Angiojet Ultra 5000a Console (2019-11-11)
Archived0
CategoryMedical devices
Last updated2019-12-13
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert