Home/Recalls/CANADA-57858
Health CanadaType II

PENTAX Video Duodenoscope (2018-02-20)

Published: February 22, 2018Recall ID: 57858Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

PENTAX Video Duodenoscope (2018-02-20)

Additional Source Details

FieldValue
N I D57858
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/pentax-video-duodenoscope-2018-02-20
IssueMedical devices
Title PENTAX Video Duodenoscope (2018-02-20)
Archived0
CategoryMedical devices
Last updated2018-02-22
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert