Philips Respironics announced a voluntary recall for certain CPAP, BiLevel PAP and Ventilator Devices due to two issues related to the sound abatement foam used in these devices.

To register your device for repair or replacement, please go to philips.com/src-update or call Philips Respironics at 877-907-7508. This website also has information on the Recall Notice and a complete list of impacted products.

We expect further direction from national medical authorities shortly. Once we have this information we will reach out to affected patients with further instructions.

Please note this recall applies to Philips Respironics devices only. We have received no warnings or communication about issues with Resmed or other manufacturer’s devices.