Home/Recalls/CANADA-52987
Health CanadaType III

Allura Xper FD10 (2014-12-09)

Published: December 23, 2014Recall ID: 52987Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

Allura Xper FD10 (2014-12-09)

Additional Source Details

FieldValue
N I D52987
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/allura-xper-fd10-2014-12-09
IssueMedical devices
Title Allura Xper FD10 (2014-12-09)
Archived1
CategoryMedical devices
Last updated2014-12-23
OrganizationMedical devices
Recall classType III

Overview

  • Recalling FirmMedical devices
  • Risk LevelType III
Official Agency Alert