Home/Recalls/CANADA-53716
Health CanadaType III

ALLURA XPER FD20/20 (2015-08-24)

Published: September 8, 2015Recall ID: 53716Category: generalCountry: Canada

Reason for Recall / Hazard

Health products

Product Description & Identification

ALLURA XPER FD20/20 (2015-08-24)

Additional Source Details

FieldValue
N I D53716
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/allura-xper-fd2020-2015-08-24
IssueHealth products
Title ALLURA XPER FD20/20 (2015-08-24)
Archived1
CategoryMedical devices
Last updated2015-09-08
OrganizationMedical devices
Recall classType III

Overview

  • Recalling FirmMedical devices
  • Risk LevelType III
Official Agency Alert