Philips Respironics Sleep and Respiratory Care devices. In June 2021, after discovering a potential health risk related to the foam in certain CPAP, BiPAP and Mechanical Ventilator devices, Philips Respironics issued a voluntary Field Safety Notice (outside U.S.) / voluntary recall notification (U.S. only).

Nov 20, 2024 · In June 2021, Philips Respironics (Philips) recalled certain ventilators, bi-level positive airway pressure (also known as Bilevel PAP, BiPAP, or BPAP) machines, and continuous positive airway...

Jul 3, 2022 · How Can We Help You? Here is how to identify your Philips-Respironics CPAP Machine.

Mar 21, 2025 · In June of 2021, CPAP.com was notified by Philips Respironics of a recall for certain CPAP, APAP, and BiPAP devices, including the very popular DreamStation. We have kept our customers updated on the situation since those early days.

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.

In June 2021, Philips Respironics initiated a voluntary recall notification 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.

Contact and support options for patients impacted by the June 2021 voluntary recall of certain CPAP, BiPAP and mechanical ventilators related to PE-PUR sound abatement foam. Please note, dependent on which customer care team you need to speak with, we may be experiencing a high volume of calls and wait times may be longer than normal.

Philips is recalling certain reworked Philips DreamStations because some devices were assigned incorrect or duplicate serial numbers during initial programming. This duplication can cause...

Locate the Serial Number on Your Device. There will be a label on the bottom of your device. Locate that and on that label, there will be a series of numbers that follow a SN or S/N pattern. These are the numbers you will be needing to find out if the CPAP device that you are using is part of the Phillips recall. Complete the Registration.

In June 2021, after discovering a potential health risk related to a part in certain CPAP, BiPAP and Mechanical Ventilator devices, Philips issued a voluntary Field Safety Notice (outside U.S.) / voluntary recall notification (U.S. only).