MEDICAL DEVICE RECALL NOTIFICATION
Philips Respironics announced a Voluntary Medical Device Recall Notification for Continuous and Non-Continuous Ventilators (certain CPAP, Bilevel PAPand Ventilator Devices) due to 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, visit philips.com/src-update.
Philips Respironics encourages patients and caregivers to look up their device using the serial number and begin the claim process if affected.