Home/Recalls/CANADA-77991
Health CanadaType II

LIFEPAK 35 Monitor/Defibrillator

Published: August 27, 2025Recall ID: 77991Category: generalCountry: Canada

Reason for Recall / Hazard

Performance

Product Description & Identification

LIFEPAK 35 Monitor/Defibrillator

Additional Source Details

FieldValue
N I D77991
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/lifepak-35-monitordefibrillator
IssuePerformance
TitleLIFEPAK 35 Monitor/Defibrillator
ProductLIFEPAK 35 Monitor/Defibrillator
Archived0
CategoryCardiovascular
Last updated2025-08-27
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert