Home/Recalls/CANADA-58783
Health CanadaType II

Xper Flex Cardio Physiomonitoring System-Main Unit (2018-11-18)

Published: November 30, 2018Recall ID: 58783Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

Xper Flex Cardio Physiomonitoring System-Main Unit (2018-11-18)

Additional Source Details

FieldValue
N I D58783
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/xper-flex-cardio-physiomonitoring-system-main-unit-2018-11-18
IssueMedical devices
Title Xper Flex Cardio Physiomonitoring System-Main Unit (2018-11-18)
Archived0
CategoryMedical devices
Last updated2018-11-30
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert