Philips Respironics announced a voluntary recall for Continuous and Non-Continuous Ventilators (certain CPAP, BiLevel PAP and Ventilator Devices) due to two issues related to the polyester-based polyurethane (PE-PUR) sound abatement foam used in these devices. For information on the Recall Notice, a complete list of impacted products, and potential health risks, for further information please visit: philips.com/src-update
FAQ on affected devices can be found by clicking here
To check if your device is affected, you may register your device here: Home | Philips Recall (expertinquiry.com)
If your device is part of the recall, you will be prompted to fill out an additional information form to start the recall process.
You may also call Philips Respironics directly at 877-907-7508, Monday-Friday 8AM to 8PM EST or click here to access Respironics Patient Portal.
We will update this page with additional information as it becomes available.