Home/Recalls/CANADA-59101
Health CanadaType III

VITEK MS (2019-04-19)

Published: May 17, 2019Recall ID: 59101Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

VITEK MS (2019-04-19)

Additional Source Details

FieldValue
N I D59101
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/vitek-ms-2019-04-19
IssueMedical devices
Title VITEK MS (2019-04-19)
Archived0
CategoryMedical devices
Last updated2019-05-17
OrganizationMedical devices
Recall classType III

Overview

  • Recalling FirmMedical devices
  • Risk LevelType III
Official Agency Alert