Home/Recalls/CANADA-52775
Health CanadaType III

ALLURA XPER FD10/10, FD20/10, FD10, FD20 Main Units (2015-02-05)

Published: March 5, 2015Recall ID: 52775Category: generalCountry: Canada

Reason for Recall / Hazard

Health products

Product Description & Identification

ALLURA XPER FD10/10, FD20/10, FD10, FD20 Main Units (2015-02-05)

Additional Source Details

FieldValue
N I D52775
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/allura-xper-fd1010-fd2010-fd10-fd20-main-units-2015-02-05
IssueHealth products
Title ALLURA XPER FD10/10, FD20/10, FD10, FD20 Main Units (2015-02-05)
Archived1
CategoryMedical devices
Last updated2015-03-05
OrganizationMedical devices
Recall classType III

Overview

  • Recalling FirmMedical devices
  • Risk LevelType III
Official Agency Alert