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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. 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.
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).
The last day to register an affected CPAP / BiPAP device in the US and Canada is 11:59pm EST, December 31, 2024. Patients who have not registered an affected device should do so before the registration end date.
The issue relates to certain ventilators, Philips CPAP (Continuous Positive Airway Pressure) and BiPap (Bi-Level Positive Airway Pressure) sleep apnea devices. All Affected Devices Manufactured Before 26 April 2021, All Device Serial Numbers. Continuous Ventilator, Minimum Ventilatory Support, Facility Use.
Which sleep and respiratory care products are affected by the recall notification/field safety notice*? The affected CPAP, BiPAP sleep therapy and ventilator devices can be found at www.philips.com/src-update. The CPAP and BiPAP sleep therapy devices represent the vast majority of the registered affected devices globally.
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.
