Home/Recalls/CANADA-57561
Health CanadaType II

VITEK 2 GP ID (2017-10-16)

Published: October 30, 2017Recall ID: 57561Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

VITEK 2 GP ID (2017-10-16)

Additional Source Details

FieldValue
N I D57561
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/vitek-2-gp-id-2017-10-16
IssueMedical devices
Title VITEK 2 GP ID (2017-10-16)
Archived1
CategoryMedical devices
Last updated2017-10-30
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert