Home/Recalls/CANADA-63647
Health CanadaType II

ALLURA XPER FD10 and FD20/10 (PRODUCT OF ALLURACLARITY FAMILY)

Published: November 25, 2021Recall ID: 63647Category: generalCountry: Canada

Reason for Recall / Hazard

Software defect

Product Description & Identification

ALLURA XPER FD10 and FD20/10 (PRODUCT OF ALLURACLARITY FAMILY)

Additional Source Details

FieldValue
N I D63647
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/allura-xper-fd10-and-fd2010-product-alluraclarity-family
IssueSoftware defect
TitleALLURA XPER FD10 and FD20/10 (PRODUCT OF ALLURACLARITY FAMILY)
ProductALLURA XPER FD10 and FD20/10 (PRODUCT OF ALLURACLARITY FAMILY)
Archived0
CategoryRadiology
Last updated2021-11-25
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert