Home/Recalls/CANADA-56391
Health CanadaType II

Artis Devices (2016-12-14)

Published: January 6, 2017Recall ID: 56391Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

Artis Devices (2016-12-14)

Additional Source Details

FieldValue
N I D56391
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/artis-devices-2016-12-14
IssueMedical devices
Title Artis Devices (2016-12-14)
Archived1
CategoryMedical devices
Last updated2017-01-06
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert