Home/Recalls/CANADA-51020
Health CanadaType III

Unicel DXH 600 and 800 Systems (2013-10-31)

Published: December 17, 2013Recall ID: 51020Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

Unicel DXH 600 and 800 Systems (2013-10-31)

Additional Source Details

FieldValue
N I D51020
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/unicel-dxh-600-and-800-systems-2013-10-31
IssueMedical devices
Title Unicel DXH 600 and 800 Systems (2013-10-31)
Archived1
CategoryMedical devices
Last updated2013-12-17
OrganizationMedical devices
Recall classType III

Overview

  • Recalling FirmMedical devices
  • Risk LevelType III
Official Agency Alert