Home/Recalls/CANADA-82292
Health CanadaType II

Allura Xper FD10

Published: July 8, 2026Recall ID: 82292Category: generalCountry: Canada

Reason for Recall / Hazard

Performance

Product Description & Identification

Allura Xper FD10

Additional Source Details

FieldValue
N I D82292
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/allura-xper-fd10
IssuePerformance
TitleAllura Xper FD10
ProductAllura Xper FD10
Archived0
CategoryRadiology
Last updated2026-07-08
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert