What the what?
Philips Respironics announced a voluntary recall for Continuous and Non-Continuous Ventilators (certain CPAP, Bi-Level PAP and Ventilator Devices) due to two issues related to the polyester-based polyurethane (PE-PUR) sound abatement foam used in these devices. Please also reach out to your physician with any additional questions you may have regarding your medical therapy. For information on the Recall Notice, a complete list of impacted products, and potential health risks, visit https://www.usa.philips.com/healthcare/e/sleep/communications/src-update
Please contact our office with any product questions (877-487-2782).
