Home/Recalls/CANADA-81234
Health CanadaType II

Philips IntelliVue Patient Monitors

Published: February 20, 2026Recall ID: 81234Category: generalCountry: Canada

Reason for Recall / Hazard

Performance

Product Description & Identification

Philips IntelliVue Patient Monitors

Additional Source Details

FieldValue
N I D81234
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/philips-intellivue-patient-monitors
IssuePerformance
TitlePhilips IntelliVue Patient Monitors
ProductPhilips IntelliVue Patient Monitors
Archived0
CategoryCardiovascular - General hospital and personal use
Last updated2026-02-20
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert