Voluntary Recall Information

Philips Respironics Sleep and Respiratory Care devices

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News and Updates > Remediation progress update

Remediation progress update

April 10, 2024

Completing the Philips Respironics medical device recall remains our highest priority. With the remediation of the sleep therapy devices almost complete and remediation of the ventilators ongoing, it is important that patients, Durable Medical Equipment providers (DMEs) and clinicians are informed on the latest updates.

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Ventilation device remediation progress updates


We are committed to remediating affected ventilators in alignment with the relevant competent authorities, and continue to work with independent testing laboratories to conduct extensive testing and analysis of the affected devices.


Philips Respironics will communicate with DMEs directly throughout the remediation process. If you are a patient or caregiver with an affected Philips Respironics ventilation device, you do not need to take any action. All ventilation remediation will be done via your DME.

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Sleep therapy device remediation progress updates


Globally, we have remediated 99% of actionable* sleep therapy device registrations to date. 

Continuing to remediate new and existing registrations remains our priority. We will make multiple attempts to ensure we have the information needed to place an order, and will provide responding patients with remediation options. 

2.61 million


US actionable* registrations.

Information as of Mar. 27, 2024

2.59 million


patients** remediated in the US.

Information as of Mar. 27, 2024

*Actionable registrations are those that contain the necessary information needed to complete the remediation and are not awaiting further information.

** Remediated patients include those who have received a new, recertified or an alternative device sent as replacements for affected units, those who have had devices shipped to their DME directly handling patient remediations, or those who received financial payment.

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