Home/Recalls/CANADA-77487
Health CanadaType II

EVIS EXERA III Duodenovideoscope

Published: May 22, 2025Recall ID: 77487Category: generalCountry: Canada

Reason for Recall / Hazard

Labelling and packaging

Product Description & Identification

EVIS EXERA III Duodenovideoscope

Additional Source Details

FieldValue
N I D77487
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/evis-exera-iii-duodenovideoscope-0
IssueLabelling and packaging
TitleEVIS EXERA III Duodenovideoscope
ProductEVIS EXERA III Duodenovideoscope
Archived0
CategoryGastroenterology and urology
Last updated2025-05-22
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert