Home/Recalls/CANADA-58720
Health CanadaType III

UniCel DxC 600, 600i, 800, 800i, 860i, 880i (2018-10-29)

Published: February 15, 2019Recall ID: 58720Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

UniCel DxC 600, 600i, 800, 800i, 860i, 880i (2018-10-29)

Additional Source Details

FieldValue
N I D58720
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/unicel-dxc-600-600i-800-800i-860i-880i-2018-10-29
IssueMedical devices
Title UniCel DxC 600, 600i, 800, 800i, 860i, 880i (2018-10-29)
Archived0
CategoryMedical devices
Last updated2019-02-15
OrganizationMedical devices
Recall classType III

Overview

  • Recalling FirmMedical devices
  • Risk LevelType III
Official Agency Alert