Home/Recalls/CANADA-58672
Health CanadaType I

LIFEPAK 15 Monitor/Defibrillator (2019-01-29)

Published: February 12, 2019Recall ID: 58672Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

LIFEPAK 15 Monitor/Defibrillator (2019-01-29)

Additional Source Details

FieldValue
N I D58672
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/lifepak-15-monitordefibrillator-2019-01-29
IssueMedical devices
Title LIFEPAK 15 Monitor/Defibrillator (2019-01-29)
Archived0
CategoryMedical devices
Last updated2019-02-12
OrganizationMedical devices
Recall classType I

Overview

  • Recalling FirmMedical devices
  • Risk LevelType I
Official Agency Alert