Home/Recalls/CANADA-57631
Health CanadaType II

CoaguChek XS Pro and Plus, Cobas H 232 Instruments (2017-12-18)

Published: January 29, 2018Recall ID: 57631Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

CoaguChek XS Pro and Plus, Cobas H 232 Instruments (2017-12-18)

Additional Source Details

FieldValue
N I D57631
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/coaguchek-xs-pro-and-plus-cobas-h-232-instruments-2017-12-18
IssueMedical devices
Title CoaguChek XS Pro and Plus, Cobas H 232 Instruments (2017-12-18)
Archived0
CategoryMedical devices
Last updated2018-01-29
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert