Home/Recalls/CANADA-62729
Health CanadaGeneral Alert

Philips Respironics recalls several models of CPAP and BiLevel PAP machines and ...

Published: July 5, 2024Recall ID: 62729Category: generalCountry: Canada

Reason for Recall / Hazard

Performance

Product Description & Identification

Register your device on the Philips recall website or call its recall hotline at 1-877-907-7508. Philips has established a registration process where you can look up your device serial number and begin a claim if your unit is affected.If you have an affected product talk to your physician, or medical device provider first before stopping or changing how you use your product, as the benefits of using these devices may outweigh the risks for many users.Be sure to clean your device only according to the manufacturer’s Instructions for Use, as the use of non-validated cleaning methods (e.g. ozone) could contribute to potential foam degradation.Do not attempt to remove or replace the foam yourself.Report any health product-related side effects or complaints to Health Canada.

Affected Products

Philips Respironics Continuous Positive Airway Pressure (CPAP) machines, BiLevel Positive Airway Pressure (BiLevel PAP) machines and mechanical ventilators

Additional Source Details

FieldValue
N I D62729
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/philips-respironics-recalls-several-models-cpap-and-bilevel-pap-machines-and
IssuePerformance
Title Philips Respironics recalls several models of CPAP and BiLevel PAP machines and mechanical ventilators
ProductPhilips Respironics Continuous Positive Airway Pressure (CPAP) machines, BiLevel Positive Airway Pressure (BiLevel PAP) machines and mechanical ventilators
Archived0
CategoryMedical devices
Last updated2024-07-05
OrganizationCommunications and Public Affairs Branch
What you should doRegister your device on the Philips recall website or call its recall hotline at 1-877-907-7508. Philips has established a registration process where you can look up your device serial number and begin a claim if your unit is affected.If you have an affected product talk to your physician, or medical device provider first before stopping or changing how you use your product, as the benefits of using these devices may outweigh the risks for many users.Be sure to clean your device only according to the manufacturer’s Instructions for Use, as the use of non-validated cleaning methods (e.g. ozone) could contribute to potential foam degradation.Do not attempt to remove or replace the foam yourself.Report any health product-related side effects or complaints to Health Canada.

Overview

  • Recalling FirmCommunications and Public Affairs Branch
Official Agency Alert