Home/Recalls/CANADA-61648
Health CanadaType II

Uroskop Omnia & Uroskop Omnia Max (2020-09-11)

Published: October 2, 2020Recall ID: 61648Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

Uroskop Omnia & Uroskop Omnia Max (2020-09-11)

Additional Source Details

FieldValue
N I D61648
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/uroskop-omnia-uroskop-omnia-max-2020-09-11
IssueMedical devices
Title Uroskop Omnia & Uroskop Omnia Max (2020-09-11)
Archived0
CategoryMedical devices
Last updated2020-10-02
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert