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, visit philips.com/src-update. Patients will be receiving correspondence from Philips Respironics regarding the recall and if they own their device, they can register it online for repair/replacement. Please contact our office with any questions.