Home/Recalls/CANADA-57539
Health CanadaType II

ABL800 FLEX SYSTEM - INSTRUMENT CONFIGURATIONS (2017-10-02)

Published: October 27, 2017Recall ID: 57539Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

ABL800 FLEX SYSTEM - INSTRUMENT CONFIGURATIONS (2017-10-02)

Additional Source Details

FieldValue
N I D57539
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/abl800-flex-system-instrument-configurations-2017-10-02
IssueMedical devices
Title ABL800 FLEX SYSTEM - INSTRUMENT CONFIGURATIONS (2017-10-02)
Archived1
CategoryMedical devices
Last updated2017-10-27
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert