Home/Recalls/CANADA-58980
Health CanadaType II

Uroskop Omnia, Uroskop Omnia Max (2019-02-07)

Published: February 22, 2019Recall ID: 58980Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

Uroskop Omnia, Uroskop Omnia Max (2019-02-07)

Additional Source Details

FieldValue
N I D58980
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/uroskop-omnia-uroskop-omnia-max-2019-02-07
IssueMedical devices
Title Uroskop Omnia, Uroskop Omnia Max (2019-02-07)
Archived0
CategoryMedical devices
Last updated2019-02-22
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert