Home/Recalls/CANADA-50453
Health CanadaType III

Axiom Luminos DRF System - Main Unit and Uroskop Omnia (2013-09-02)

Published: October 16, 2013Recall ID: 50453Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

Axiom Luminos DRF System - Main Unit and Uroskop Omnia (2013-09-02)

Additional Source Details

FieldValue
N I D50453
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/axiom-luminos-drf-system-main-unit-and-uroskop-omnia-2013-09-02
IssueMedical devices
Title Axiom Luminos DRF System - Main Unit and Uroskop Omnia (2013-09-02)
Archived1
CategoryMedical devices
Last updated2013-10-16
OrganizationMedical devices
Recall classType III

Overview

  • Recalling FirmMedical devices
  • Risk LevelType III
Official Agency Alert