Philips Respironics Sleep and Respiratory Care devices
Sleep therapy device patients can get updates on a registered device by visiting the Patient Portal. If you are a patient or caregiver with an affected Philips Respironics ventilation device, you do not need to take any action.
Information for patients
Patient safety is our top priority. We are committed to completing the remediation for all affected patients to make sure you receive safe and effective therapy.
If you are a patient or caregiver with an affected Philips Respironics ventilation device, you do not need to take any action at this time. Philips Respironics will communicate with Durable Medical Equipment providers (DMEs) directly throughout the ventilation device remediation process.
If you registered an affected CPAP / BiPAP device and are still waiting for your replacement, it is likely because we need important information or consent from you. Without this information, we are unable to ship your replacement CPAP / BiPAP device. Depending on your affected registered device, you may have alternative options.
Learn about my options
Ozone and UV light cleaning products are not currently approved cleaning methods for sleep apnea devices or masks and should not be used.
Ozone Cleaner Information
Latest updates
Explained: The voluntary Philips Respironics sleep and respiratory care devices recall*
* This is a voluntary recall notification in the US and field safety notice in other countries
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Explained: The Philips Respironics Consent Decree
April 4, 2024
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Philips response to recent media articles related to Philips Respironics’ voluntary recall notification/field safety notice
September 27, 2023
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All news and updates