Home/Recalls/CANADA-55300
Health CanadaType III

IVOCLAR VIVADENT AG products (2016-07-01)

Published: July 19, 2016Recall ID: 55300Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

IVOCLAR VIVADENT AG products (2016-07-01)

Additional Source Details

FieldValue
N I D55300
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/ivoclar-vivadent-ag-products-2016-07-01
IssueMedical devices
Title IVOCLAR VIVADENT AG products (2016-07-01)
Archived1
CategoryMedical devices
Last updated2016-07-19
OrganizationMedical devices
Recall classType III

Overview

  • Recalling FirmMedical devices
  • Risk LevelType III
Official Agency Alert