Home/Recalls/CANADA-61240
Health CanadaType II

CardioLab System - Amplifier (2018-09-17)

Published: May 8, 2020Recall ID: 61240Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

CardioLab System - Amplifier (2018-09-17)

Additional Source Details

FieldValue
N I D61240
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/cardiolab-system-amplifier-2018-09-17
IssueMedical devices
Title CardioLab System - Amplifier (2018-09-17)
Archived0
CategoryMedical devices
Last updated2020-05-08
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert