On June 14, 2021, Philips issued a recall notice for specific BiLevel PAP and CPAP devices.

For patients using Philips BiLevel PAP and CPAP devices: Discontinue use of affected units and consult with physicians to determine the benefits of continuing therapy and potential risks.

Click here for a list of affected devices and further steps patients should take.

Click here for answers to Frequently Asked Questions concerning why the affected units have been recalled, the safety issues involved, the corrective steps that are being taken, and more.

We will continue to provide updates on this product recall as additional information becomes available.