Home/Recalls/CANADA-57839
Health CanadaType II

XPER FLEX CARDIO PHYSIOMONITORING SYSTEM - MAIN UNIT (2017-11-14)

Published: December 14, 2017Recall ID: 57839Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

XPER FLEX CARDIO PHYSIOMONITORING SYSTEM - MAIN UNIT (2017-11-14)

Additional Source Details

FieldValue
N I D57839
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/xper-flex-cardio-physiomonitoring-system-main-unit-2017-11-14
IssueMedical devices
Title XPER FLEX CARDIO PHYSIOMONITORING SYSTEM - MAIN UNIT (2017-11-14)
Archived1
CategoryMedical devices
Last updated2017-12-14
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert