Home/Recalls/CANADA-63991
Health CanadaType II

Exalt Model D Single-Use Duodenoscope

Published: March 14, 2022Recall ID: 63991Category: generalCountry: Canada

Reason for Recall / Hazard

Revised instructions for use

Product Description & Identification

Exalt Model D Single-Use Duodenoscope

Additional Source Details

FieldValue
N I D63991
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/exalt-model-single-use-duodenoscope
IssueRevised instructions for use
TitleExalt Model D Single-Use Duodenoscope
ProductExalt Model D Single-Use Duodenoscope
Archived0
CategoryGastroenterology and urology
Last updated2022-03-14
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert