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. We will continue to prioritize remediation of registered sleep and respiratory care devices and will also continue to accept returned affected devices at no cost.
If you have questions on the closure of affected device registration or the US Patient Portal closure, please contact [email protected] and provide your name, phone number, shipping address (we cannot accept P.O. boxes), affected device serial number and your specific question. Failure to provide this information could lead to a delay in response.
As of October 16, 2026, we have completed all the remediation steps required by the US Recall Remediation Plan related to the June 2021 recall for Mechanical Ventilator devices.
Using current remediation options, we will continue to respond to and remediate registered affected devices. The ongoing availability of remediation options is subject to change.
As of October 16, 2026:
US actionable* registrations: 102,000
Devices** remediated in the US: 102,000
* Actionable registrations are those that contain the necessary information needed to complete the remediation and devices are in possession of customer.
** Figure reflects remediation through financial compensation program, or a device rework remediation option.
Click here for ventilation news and updates.
Globally, we have remediated 99% of actionable* sleep therapy device registrations to date.
As of July 6, 2026 we have completed all the remediation steps required by the US Recall Remediation Plan related to the June 2021 recall for sleep therapy devices.
Using current remediation options, we will continue to respond to and remediate registered affected devices. The ongoing availability of remediation options remains subject to change.
As of October 16, 2026:
US actionable* registrations: 2.685 million
Patients** remediated in the US: 2.685 million
* 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.