Home/Recalls/CANADA-53492
Health CanadaType III

ALLURA XPER FD20 (2014-12-09)

Published: April 13, 2015Recall ID: 53492Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

ALLURA XPER FD20 (2014-12-09)

Additional Source Details

FieldValue
N I D53492
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/allura-xper-fd20-2014-12-09
IssueMedical devices
Title ALLURA XPER FD20 (2014-12-09)
Archived1
CategoryMedical devices
Last updated2015-04-13
OrganizationMedical devices
Recall classType III

Overview

  • Recalling FirmMedical devices
  • Risk LevelType III
Official Agency Alert