Home/Recalls/CANADA-59240
Health CanadaType III

Perimeter Octopus 900 (2019-06-10)

Published: June 21, 2019Recall ID: 59240Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

Perimeter Octopus 900 (2019-06-10)

Additional Source Details

FieldValue
N I D59240
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/perimeter-octopus-900-2019-06-10
IssueMedical devices
Title Perimeter Octopus 900 (2019-06-10)
Archived0
CategoryMedical devices
Last updated2019-06-21
OrganizationMedical devices
Recall classType III

Overview

  • Recalling FirmMedical devices
  • Risk LevelType III
Official Agency Alert