Home/Recalls/CANADA-74439
Health CanadaType II

Exalt Model D Single-Use Duodenoscope

Published: October 18, 2023Recall ID: 74439Category: generalCountry: Canada

Reason for Recall / Hazard

Performance

Product Description & Identification

Exalt Model D Single-Use Duodenoscope

Additional Source Details

FieldValue
N I D74439
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/exalt-model-single-use-duodenoscope-0
IssuePerformance
TitleExalt Model D Single-Use Duodenoscope
ProductExalt Model D Single-Use Duodenoscope
Archived0
CategoryGastroenterology and urology
Last updated2023-10-18
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert