Home/Recalls/CANADA-55773
Health CanadaType II

IONTODERMA ID-1000 (2016-08-08)

Published: August 10, 2016Recall ID: 55773Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

IONTODERMA ID-1000 (2016-08-08)

Additional Source Details

FieldValue
N I D55773
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/iontoderma-id-1000-2016-08-08
IssueMedical devices
Title IONTODERMA ID-1000 (2016-08-08)
Archived1
CategoryMedical devices
Last updated2016-08-10
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert