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Urgent: Medical Device Recall
Philips Respironics CPAP and Bi-Level PAP Devices

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. For information on the Recall Notice, a complete list of impacted products, and potential health risks, visit philips.com/src-update. Please contact Respironics with any questions at 1-877-907-7508.