Recalled Philips Devices: Is Your CPAP or BiPAP on the List?
The June 2021 Philips Respironics recall covers a wide range of CPAP, BiPAP, and ventilator models. Check if your device is affected and what that means for your settlement eligibility.
⚠ Class I Recall: The FDA has classified this as the most serious type of recall. Use of affected devices may cause serious adverse health consequences or death. If you used any of the devices listed below, you may be eligible for compensation through the settlement program.
CPAP Devices Recalled
- DreamStation CPAP (all variants)
- DreamStation Go (travel CPAP)
- DreamStation 2 (newer generation)
- SystemOne CPAP (Q-Series, 50 Series, 60 Series)
- REMstar SE Auto
- REMstar Plus
- REMstar Auto
- REMstar Pro
- Dorma 400
- Dorma 500
BiPAP / BiLevel PAP Devices Recalled
- DreamStation BiPAP Auto
- DreamStation BiPAP AVAPS
- DreamStation Go BiPAP Auto
- SystemOne BiPAP Auto
- A-Series BiPAP Hybrid A30
- A-Series BiPAP A30
- A-Series BiPAP A40
- A-Series BiPAP V30 Auto
- C-Series S/T
- C-Series AVAPS
- DuoLab
- OmniLab Advanced+
Ventilators & Other Devices Recalled
- Trilogy 100 (mechanical ventilator)
- Trilogy 200 (mechanical ventilator)
- Garbin Plus, Aeris, LifeVent
- Harmony II
- Stardust II
Note on DreamStation 2: Some DreamStation 2 devices use a different silicone-based foam that is NOT subject to the same degradation concern. However, DreamStation 2 devices with PE-PUR foam are still included. Check the device label and serial number.
How to Check if Your Device Is Recalled
- Find your device model — Check the label on the side or bottom of your CPAP machine
- Find your serial number — Usually on a sticker on the bottom or back of the device
- Check FDA records — The FDA maintains a list of recalled devices with serial number ranges at fda.gov (search "Philips CPAP recall")
- Check Philips' registration — Philips maintains a recall registration at philipsrecallregistration.com
- Ask your DME supplier — The company that provided your device may have recall records
If Your Device Was Recalled and You Don't Have It Anymore
Many people already returned, discarded, or stopped using their Philips CPAP. You do not need to currently possess the device to file a claim. Documentation that can establish your device ownership includes:
- Prescription records from your sleep physician
- Purchase receipts or insurance EOB (Explanation of Benefits)
- DME (durable medical equipment) supplier records
- VA records (for veterans who received the device through the VA)
- Philips recall registration confirmation emails
- Photos of the device before disposal
- Insurance records showing CPAP supplies were covered
Not Sure If You Have a Recalled Device?
If you used a Philips-branded CPAP or BiPAP device between approximately 2009 and 2021, there is a significant probability it falls within the recall. The device models above cover the vast majority of Philips Respironics consumer CPAP and BiPAP products sold during that period.
An attorney can help you verify your device's recall status and evaluate your eligibility for both the economic loss and personal injury settlement tracks.
Used Any of These Devices? Check Your Eligibility.
If your device is on this list — or if you're not sure — a free eligibility check can determine which settlement track(s) you qualify for. The process takes 2 minutes.
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