Home/Recalls/CANADA-59072
Health CanadaType II

Automated Endoscope Reprocessor (2019-02-19)

Published: March 15, 2019Recall ID: 59072Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

Automated Endoscope Reprocessor (2019-02-19)

Additional Source Details

FieldValue
N I D59072
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/automated-endoscope-reprocessor-2019-02-19
IssueMedical devices
Title Automated Endoscope Reprocessor (2019-02-19)
Archived0
CategoryMedical devices
Last updated2019-03-15
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert