Home/Recalls/CANADA-59175
Health CanadaType III

Ysio Max, Luminos dRF Max, Uroskop Omnia Max (2019-05-08)

Published: May 31, 2019Recall ID: 59175Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

Ysio Max, Luminos dRF Max, Uroskop Omnia Max (2019-05-08)

Additional Source Details

FieldValue
N I D59175
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/ysio-max-luminos-drf-max-uroskop-omnia-max-2019-05-08
IssueMedical devices
Title Ysio Max, Luminos dRF Max, Uroskop Omnia Max (2019-05-08)
Archived0
CategoryMedical devices
Last updated2019-05-31
OrganizationMedical devices
Recall classType III

Overview

  • Recalling FirmMedical devices
  • Risk LevelType III
Official Agency Alert