Home/Recalls/CANADA-54624
Health CanadaType II

PENTAX VIDEO DUODENOSCOPE (2016-03-03)

Published: March 17, 2016Recall ID: 54624Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

PENTAX VIDEO DUODENOSCOPE (2016-03-03)

Additional Source Details

FieldValue
N I D54624
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/pentax-video-duodenoscope-2016-03-03
IssueMedical devices
Title PENTAX VIDEO DUODENOSCOPE (2016-03-03)
Archived1
CategoryMedical devices
Last updated2016-03-17
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert