Home/Recalls/CANADA-51013
Health CanadaType I

Veris 8600 Vital Signs Monitor - Systems (2013-11-20)

Published: January 13, 2014Recall ID: 51013Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

Veris 8600 Vital Signs Monitor - Systems (2013-11-20)

Additional Source Details

FieldValue
N I D51013
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/veris-8600-vital-signs-monitor-systems-2013-11-20
IssueMedical devices
Title Veris 8600 Vital Signs Monitor - Systems (2013-11-20)
Archived1
CategoryMedical devices
Last updated2014-01-13
OrganizationMedical devices
Recall classType I

Overview

  • Recalling FirmMedical devices
  • Risk LevelType I
Official Agency Alert