Philips Voluntary Recall on CPAP, BiLevel PAP & Ventilators

June 17, 2021

We are committed to serving our patients in a responsible and safe manner. We are aware of the voluntary recall from Philips Respironics regarding the issues related to sound abatement foam used in certain CPAP, BiLevel PAP and ventilator devices and are working diligently to resolve this issue as soon as possible.

We are currently waiting for Philips Respironics to notify us of the proper recall process and will be reaching out to our patients in the coming days as more information is available.

Philips has created a registration process that will allow you​ to look up your device serial number and identify if your unit is affected.

Please go to the Philips Respironics recall website at or call 877-907-7508 for more information.