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Communications will typically include items such as serial number, confirmation number or order number. For further information about your current status, please log into the portal or call 877-907-7508.
We appreciate your cooperation and patience and encourage you to save your registration confirmation number for future communications. To check the status of your replacement CPAP or BiPAP device, please be sure to visit the Patient Portal .
Voluntary Recall Information. Philips Respironics Sleep and Respiratory Care devices. Registration for affected CPAP and BiPAP devices in the US and Canada ends at 11:59 p.m. EST, December 31, 2024. Register now. Learn more. Important information for clinicians. Sleep Therapy information.
29 sty 2024 · In 2021, Philips Respironics determined from user reports and initial testing that there were possible risks to users related to the polyester-based polyurethane (PE-PUR) sound abatement foam used in specific CPAP, BiPAP and ventilator devices. Following the issuance of the recall
14 lis 2022 · Please see below the instructions for returning your affected device to Philips Respironics. Do not return your affected device until you have successfully setup your replacement device. Do not discard any of the packaging material.
As a result of extensive ongoing analysis, on June 14, 2021, the company issued a recall notification for specific affected Continuous Positive Airway Pressure (CPAP), Bi-Level Positive Airway Pressure (BiLevel PAP) devices, and Mechanical Ventilators.
In June 2021, Philips initiated a voluntary recall notification / field safety notice for certain CPAP and BiPAP sleep therapy devices and mechanical ventilators to address potential health risks related to the polyester-based polyurethane (PE-PUR) sound abatement foam in these devices.
