Home/Recalls/CANADA-58333
Health CanadaType II

VITROS 5600 Integrated System (2018-08-20)

Published: August 31, 2018Recall ID: 58333Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

VITROS 5600 Integrated System (2018-08-20)

Additional Source Details

FieldValue
N I D58333
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/vitros-5600-integrated-system-2018-08-20
IssueMedical devices
Title VITROS 5600 Integrated System (2018-08-20)
Archived0
CategoryMedical devices
Last updated2018-08-31
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert