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If you registered an affected CPAP / BiPAP device and are still waiting for your replacement, it is likely because we need important information or consent from you. Without this information, we are unable to ship your replacement CPAP / BiPAP device.
- Patients
If you registered an affected CPAP / BiPAP device and are...
- Business customers
Registration for affected CPAP and BiPAP devices in the US...
- Clinicians
The last day to register an affected CPAP / BiPAP device in...
- News and Updates
* This is a voluntary recall notification in the US and...
- Contact and support
Voluntary Recall Information. Philips Respironics Sleep and...
- Ozone Cleaner Information
“Follow the CPAP manufacturer’s instructions and recommended...
- Starts Repair and Replacement
Philips has received authorization from the US Food and Drug...
- Patients
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).
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.
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.
Register your device. 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).
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.
