Home/Recalls/CANADA-57716
Health CanadaType II

ALLURA XPER FD10/10 - Main Unit, FD20/10 System-Main Unit, FD20/20, FD10, FD20 S...

Published: January 29, 2018Recall ID: 57716Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

ALLURA XPER FD10/10 - Main Unit, FD20/10 System-Main Unit, FD20/20, FD10, FD20 System - Main Unit, FD20 Or Table (2017-12-28)

Additional Source Details

FieldValue
N I D57716
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/allura-xper-fd1010-main-unit-fd2010-system-main-unit-fd2020-fd10-fd20-system-main-unit
IssueMedical devices
Title ALLURA XPER FD10/10 - Main Unit, FD20/10 System-Main Unit, FD20/20, FD10, FD20 System - Main Unit, FD20 Or Table (2017-12-28)
Archived0
CategoryMedical devices
Last updated2018-01-29
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert