Home/Recalls/CANADA-59365
Health CanadaType III

MobileDiagnost wDR (2019-03-25)

Published: April 18, 2019Recall ID: 59365Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

MobileDiagnost wDR (2019-03-25)

Additional Source Details

FieldValue
N I D59365
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/mobilediagnost-wdr-2019-03-25
IssueMedical devices
Title MobileDiagnost wDR (2019-03-25)
Archived0
CategoryMedical devices
Last updated2019-04-18
OrganizationMedical devices
Recall classType III

Overview

  • Recalling FirmMedical devices
  • Risk LevelType III
Official Agency Alert