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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
Patients - Medical Device Recall Information - Philips...
- Business customers
Business customers - Medical Device Recall Information -...
- Clinicians
Clinicians - Medical Device Recall Information - Philips...
- News and Updates
* This is a voluntary recall notification in the US and...
- Contact and support
Contact and support - Medical Device Recall Information -...
- 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
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.
a. The website provides you current information on the status of the recall and how to receive permanent corrective action to address the two (2) issues. b. The website also provides you instructions on how to locate your device Serial Number and will guide you through the registration process.
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 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.
