The Philips CPAP, BiPAP & Ventilator Recall: What You Need to Know
Philips recalled millions of sleep and respiratory devices in June 2021 over a foam degradation issue. Here's which devices are affected, what's changed by 2026, and what to do if you're using one.
In this guide
What happened
In June 2021, Philips issued a recall (in the US) and a Field Safety Notice (outside the US) for millions of CPAP, BiPAP and mechanical ventilator devices. The concern was the polyurethane sound-abatement foam used inside these devices, which can degrade — particularly with heat, high humidity, or unapproved cleaning methods such as ozone or UV-light sanitisers — and potentially release particles or chemical emissions into the airway.
In the US, the FDA classified this as a Class I recall — its most serious category, reserved for situations where using the product could cause serious injury or death.
Which devices are affected
All Philips CPAP, BiPAP and ventilator devices manufactured before April 26, 2021, under any serial number, are covered by the recall. This includes:
The recall list has been amended over time — some Trilogy Evo ventilators sold as late as February 2024 were later added. Always check your exact model and serial number against Philips' current official recall information rather than relying on a device-line name alone.
What to do if you have an affected device
Talk to your doctor before stopping
If your device is life-sustaining (many ventilators are), don't stop using it without medical guidance — your doctor can advise on alternate options that won't interrupt necessary therapy.
For CPAP/BiPAP, discuss discontinuing use
For most sleep apnea CPAP and BiPAP therapy (non-life-sustaining), your doctor may recommend switching to a replacement device while your recalled unit is addressed.
Check your device's status with Philips
Philips' official remediation channels are the authoritative source for whether your specific device has been resolved, replaced, or is still pending.
Note: Philips' US Patient Portal for registering affected devices closed on January 1, 2026, and US/Canada registration closed at the end of 2024. If your device was never registered or your case is still open, current guidance is to contact Philips directly rather than through the closed portal.
Where things stand in 2026
Philips reports having remediated roughly 99% of registered sleep therapy devices globally, though remediation of ventilators is still ongoing, and the 99% figure includes repairs, physical replacements, and in some cases monetary reimbursement rather than a replacement device. Philips also discontinued new CPAP sales in the US following an April 2024 consent decree with the FDA.
Separately from the device remediation programme, a $479 million settlement (agreed in December 2023) covers economic claims for people who purchased, rented or leased certain recalled machines in the US between 2008 and 2021 — this settlement doesn't cover injury or death claims, which are handled through a separate ongoing lawsuit process.
If you're outside the US, remediation timelines and processes have varied by country. Contact Philips through your local distributor or their official communications channel for the most accurate status for your region.
Looking for a non-Philips replacement
If you're waiting on remediation or would simply prefer a different manufacturer, we carry ResMed CPAP and BiPAP machines, including the current AirSense 11 AutoSet.
Or if budget is the main concern, our budget-friendly CPAP machines guide covers affordable options.
Frequently asked questions
Is the Philips CPAP recall finished?
Not entirely. Philips reports around 99% of registered sleep therapy devices remediated as of 2026, but ventilator remediation is still ongoing, and unregistered or unresolved individual cases are still being handled. Legal proceedings related to the recall are also still active.
Should I stop using my recalled device immediately?
For life-sustaining ventilators, don't stop without first consulting your doctor, who can arrange alternate ventilation. For CPAP/BiPAP sleep apnea therapy, discuss discontinuing use and switching devices with your doctor or sleep specialist.
How do I check if my specific device is affected?
Compare your exact model name and serial number against Philips' official recall information, since coverage has been updated over time (for example, some Trilogy Evo units were added later). Don't rely on the device-line name alone.
Can I buy a new Philips CPAP machine now?
Philips discontinued new CPAP sales in the US following a 2024 consent decree with the FDA. Availability elsewhere has varied; if you'd rather avoid the question altogether, ResMed devices like the AirSense 11 are a widely used alternative.
Please note: this guide is for general information and isn't medical advice. Decisions about continuing, pausing or switching prescribed CPAP, BiPAP or ventilator therapy should always be made with your doctor or sleep specialist, and device remediation status should be confirmed directly with Philips.
