Voluntary Recall Information
Philips Respironics Sleep and Respiratory Care devices
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News and Updates > Remediation progress update
Remediation progress update
September 19, 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.
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.
133,000
US actionable* registrations. Information as of September 4, 2024
44,000
devices** remediated in the US. Information as of September 4, 2024
*Actionable registrations are those that contain the necessary information needed to complete the remediation and are not awaiting further information.
** Figure reflects those devices remediated through our financial compensation program.
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.
2.66 million
US actionable* registrations. Information as of September 4, 2024
2.64 million
patients** remediated in the US. Information as of September 4, 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.
