Home/Recalls/CANADA-60954
Health CanadaType II

Philips OmniDiagnost and OmniDiagnost Eleva (2018-05-07)

Published: May 18, 2018Recall ID: 60954Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

Philips OmniDiagnost and OmniDiagnost Eleva (2018-05-07)

Additional Source Details

FieldValue
N I D60954
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/philips-omnidiagnost-and-omnidiagnost-eleva-2018-05-07
IssueMedical devices
Title Philips OmniDiagnost and OmniDiagnost Eleva (2018-05-07)
Archived0
CategoryMedical devices
Last updated2018-05-18
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert