Home/Recalls/CANADA-55292
Health CanadaType III

Philips DuraDiagnost X-ray System (2016-06-22)

Published: July 19, 2016Recall ID: 55292Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

Philips DuraDiagnost X-ray System (2016-06-22)

Additional Source Details

FieldValue
N I D55292
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/philips-duradiagnost-x-ray-system-2016-06-22
IssueMedical devices
Title Philips DuraDiagnost X-ray System (2016-06-22)
Archived1
CategoryMedical devices
Last updated2016-07-19
OrganizationMedical devices
Recall classType III

Overview

  • Recalling FirmMedical devices
  • Risk LevelType III
Official Agency Alert