1. Medical Device Recall Notification Philips Respironics Sleep and Respiratory Care devices.2021. Available from:https://www.usa.philips.com/healthcare/e/sleep/communications/src-update
2. U.S. Food and Drug Administration. Certain Philips Respironics Ventilators BiPAP and CPAP Machines Recalled Due to Potential Health Risks: FDA Safety Communication | FDA.2021. Available from:https://www.fda.gov/medical-devices/safety-communications/certain-philips-respironics-ventilators-bipap-and-cpap-machines-recalled-due-potential-health-risks
3. American Academy of Sleep Medicine guidance in response to Philips recall of PAP devices.2021. Available from:https://aasm.org/clinical-resources/guidance-philips-recall-pap-devices
4. American Thoracic Society Philips Recall Notice Resources Page.2021. Available from:https://www.thoracic.org/members/assemblies/assemblies/srn/philips-recall-notice-resources-page/
5. Position statement from the canadian thoracic society, canadian sleep society and the canadian society of respiratory therapists;Ayas NT;Philips Respironics Device Recall,2021