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Health CanadaType II

Philips HeartStart OnSite and Home Defibrillator and HeartStart FRx Automated Ex...

Published: March 13, 2018Recall ID: 60730Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

Philips HeartStart OnSite and Home Defibrillator and HeartStart FRx Automated External Defibrillator (2018-02-23)

Additional Source Details

FieldValue
N I D60730
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/philips-heartstart-onsite-and-home-defibrillator-and-heartstart-frx-automated-external
IssueMedical devices
Title Philips HeartStart OnSite and Home Defibrillator and HeartStart FRx Automated External Defibrillator (2018-02-23)
Archived0
CategoryMedical devices
Last updated2018-03-13
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert