Philips Dream Station Recall information

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 http://philips.com/src-update. 

Please contact our office with any questions.  Also,  you can contact Philips directly at 1-877-907-7508.