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.

Replacement and/or repair of your device will be addressed by Philips Respironics, not South Central Sleep Center. A recall notice will be sent directly to the patient regarding the recall information, instructions, etc. To begin the registration process, patients or caregivers may call 877-907-7508. If you  have any other questions or concerns, please contact South Central Sleep Center at 601-426-2886.