Philips Respironics – Device Recall


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:

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 (
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

Philips: URGENT Medical Device Correction

We will update this page with additional information as it becomes available.