Home/Recalls/CANADA-57962
Health CanadaType II

LIFEPAK 20e DEFIBRILLATOR/MONITOR (2017-12-07)

Published: January 8, 2018Recall ID: 57962Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

LIFEPAK 20e DEFIBRILLATOR/MONITOR (2017-12-07)

Additional Source Details

FieldValue
N I D57962
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/lifepak-20e-defibrillatormonitor-2017-12-07
IssueMedical devices
Title LIFEPAK 20e DEFIBRILLATOR/MONITOR (2017-12-07)
Archived0
CategoryMedical devices
Last updated2018-01-08
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert