Home/Recalls/CANADA-81566
Health CanadaType I

EVIS EXERA III Duodenovideoscope

Published: February 3, 2026Recall ID: 81566Category: generalCountry: Canada

Reason for Recall / Hazard

Labelling and packaging

Product Description & Identification

EVIS EXERA III Duodenovideoscope

Additional Source Details

FieldValue
N I D81566
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/evis-exera-iii-duodenovideoscope-1
IssueLabelling and packaging
TitleEVIS EXERA III Duodenovideoscope
ProductEVIS EXERA III Duodenovideoscope
Archived0
CategoryGastroenterology and urology
Last updated2026-02-03
OrganizationMedical devices
Recall classType I

Overview

  • Recalling FirmMedical devices
  • Risk LevelType I
Official Agency Alert