PHILIPS RESPIRONICS RECALL INFORMATION

We want to make you aware of an important development related to certain CPAPs, BiLevel PAPs, and ventilators (including non-invasive and invasive ventilation) manufactured by Philips Respironics. Please be sure to read this information in detail.

On June 14, 2021, 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, a complete list of impacted products, potential health risks, and to register your device, please visit this page on the Philips website or call 877-907-7508.

Also, please see this information provided by the FDA: