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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. Information for patients ›. Information for business customers ›. Information for clinicians ›. An update on our progress.
- 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
Voluntary Recall Information Philips Respironics Sleep 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
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.
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.
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.
The CPAP and BiPAP sleep therapy devices represent most of the devices under the recall. To date, more than 99% of the sleep therapy device registrations globally that are complete and actionable have been remediated.
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.
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).
