Home/Recalls/CANADA-50170
Health CanadaType III

Unicel DXC 600 Pro and DXC 800 Pro Systems (2012-09-03)

Published: November 25, 2013Recall ID: 50170Category: generalCountry: Canada

Product Description & Identification

Unicel DXC 600 Pro and DXC 800 Pro Systems (2012-09-03)

Additional Source Details

FieldValue
N I D50170
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/unicel-dxc-600-pro-and-dxc-800-pro-systems-2012-09-03
Title Unicel DXC 600 Pro and DXC 800 Pro Systems (2012-09-03)
Archived1
CategoryMedical devices
Last updated2013-11-25
OrganizationMedical devices
Recall classType III

Overview

  • Recalling FirmMedical devices
  • Risk LevelType III
Official Agency Alert