Home/Recalls/CANADA-54257
Health CanadaType II

ALLURA XPER FD10, FD10/10, FD20, FD 20/10, and FD20/20 (2015-11-20)

Published: January 7, 2016Recall ID: 54257Category: generalCountry: Canada

Reason for Recall / Hazard

Health products

Product Description & Identification

ALLURA XPER FD10, FD10/10, FD20, FD 20/10, and FD20/20 (2015-11-20)

Additional Source Details

FieldValue
N I D54257
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/allura-xper-fd10-fd1010-fd20-fd-2010-and-fd2020-2015-11-20
IssueHealth products
Title ALLURA XPER FD10, FD10/10, FD20, FD 20/10, and FD20/20 (2015-11-20)
Archived1
CategoryMedical devices
Last updated2016-01-07
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert