Home/Recalls/CANADA-52393
Health CanadaType II

Axiom Luminos DRF System-Main Unit (2014-08-12)

Published: August 28, 2014Recall ID: 52393Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

Axiom Luminos DRF System-Main Unit (2014-08-12)

Additional Source Details

FieldValue
N I D52393
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/axiom-luminos-drf-system-main-unit-2014-08-12
IssueMedical devices
Title Axiom Luminos DRF System-Main Unit (2014-08-12)
Archived1
CategoryMedical devices
Last updated2014-08-28
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert