Home/Recalls/CANADA-50300
Health CanadaType II

Vitek MS (2013-10-07)

Published: November 25, 2013Recall ID: 50300Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

Vitek MS (2013-10-07)

Additional Source Details

FieldValue
N I D50300
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/vitek-ms-2013-10-07
IssueMedical devices
Title Vitek MS (2013-10-07)
Archived1
CategoryMedical devices
Last updated2013-11-25
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert