Home/Recalls/CANADA-50370
Health CanadaType III

Luminos DRF and YSIO (2013-09-02)

Published: September 27, 2013Recall ID: 50370Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

Luminos DRF and YSIO (2013-09-02)

Additional Source Details

FieldValue
N I D50370
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/luminos-drf-and-ysio-2013-09-02
IssueMedical devices
Title Luminos DRF and YSIO (2013-09-02)
Archived1
CategoryMedical devices
Last updated2013-09-27
OrganizationMedical devices
Recall classType III

Overview

  • Recalling FirmMedical devices
  • Risk LevelType III
Official Agency Alert