Philips CPAP & BiPAP Lawsuit
In 2021, Philips recalled several CPAP, BiPAP, and ventilator devices due to the degradation of sound abatement foam, which released toxic chemicals when exposed to heat and humidity. This posed serious health risks, including respiratory issues, cancer, and long-term illnesses.
Last updated May 25, 2026
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OVERVIEW
Philips CPAP and BiPAP Recall Lawsuit Overview
What is the Philips CPAP & BiPAP Recall?
Philips recalled millions of CPAP and BiPAP machines due to defective foam that degrades over time, releasing harmful chemicals. These toxins can cause respiratory issues and cancer.
The Health Risks
The degraded foam in Philips CPAP and BiPAP devices releases toxic chemicals like diethylene glycol and toluene diisocyanate, which are linked to respiratory issues, neurological symptoms, cancer, and chronic lung and heart damage.
Philips’ Alleged Liability
Plaintiffs claim Philips knew about the foam degradation risks but failed to warn consumers or take action. The lawsuits focus on product liability, negligence, and failure to protect public health.
Who is eligible?
Individuals who used the recalled Philips CPAP or BiPAP machines and later experienced respiratory issues, neurological problems, or a cancer diagnosis may be eligible for compensation.
The Complete Philips CPAP & BiPAP Lawsuit Guide
FREE PDF • 47 PAGES
The Complete Philips CPAP & BiPAP Lawsuit Lawsuit Guide
Everything you need to know about the recall lawsuit, explained in simple terms by legal and medical experts. This free guide covers:
LITIGATION PROGRESS
Philips CPAP & BiPAP Recall Lawsuit Timeline
April 2026
More plaintiffs receive compensation, but lien resolution delays settlement fund release.
March 2026
619 lawsuits still active in the MDL, with more plaintiffs receiving CPAP settlement checks.
January 2026
Judge sends CPAP cancer case back to Kentucky, rejecting Philips' MDL centralization efforts.
2025
Philips begins distributing $1.1B settlement for cancer and organ damage claims.
Estimated Payout
Compensation for Affected Individuals
Your Path to Compensation
If you’ve been affected by the Philips CPAP or BiPAP recall, you may be eligible for compensation through ongoing lawsuits addressing health issues caused by these defective devices.
Who’s Affected?
Anyone who used Philips CPAP, BiPAP, or ventilator devices and experienced health complications like respiratory or neurological issues may be eligible for compensation.
What You Can Expect
The lawsuits seek compensation for medical bills, lost wages, and pain and suffering. They also aim to hold Philips accountable and ensure better safety standards for consumers in the future.
*Claim outcomes depend on diagnosis, timing, and medical records. Similar cases may be valued differently based on each person’s circumstances.
Find a lab nearby
Locate certified MRI and neurology imaging centers to obtain the diagnostic records needed to support your claim.
What to request : Ask for a contrast-enhanced brain MRI specifically looking for meningioma. Request both the radiologist's report and the imaging CD both are needed for your legal claim.
The process
How it works
From submission to attorney match, every case follows the same four-step review.
Submit your case
Start by completing a brief, confidential questionnaire about your use of the recalled Philips devices and any related health issues.
Initial review
A specialist reviews your submission and checks eligibility.
Case manager call
You may be contacted to discuss medical history and records.
Attorney match
If eligible, your case may be referred to a lawyer handling similar claim.
References
SOURCES
Updated May 25, 2026
FDA Consent Decree Announcement
https://www.fda.gov/news-events/press-announcements/federal-court-enters-consent-decree-against-philips-respironics-following-recall-certain-sleep
U.S. Food and Drug Administration (FDA)
https://www.fda.gov/medical-devices/respiratory-devices/recalled-philips-ventilators-bipap-machines-and-cpap-machines
FDA Recall Classification & Safety Alerts
https://www.fda.gov/medical-devices/recalled-philips-ventilators-bipap-machines-and-cpap-machines/fda-activities-related-recalled-philips-ventilators-bipap-machines-and-cpap-machine
FDA Medical Device Reports Update
https://www.fda.gov/medical-devices/recalled-philips-ventilators-bipap-machines-and-cpap-machines/problems-reported-recalled-philips-ventilators-bipap-machines-and-cpap-machines
Judicial Panel on Multidistrict Litigation (JPML)
CM/ECF for JPML (LIVE)
FDA Foam Testing Summary for Recalled Devices
https://www.fda.gov/medical-devices/recalled-philips-ventilators-bipap-machines-and-cpap-machines/foam-testing-summary-recalled-philips-ventilators-bipap-machines-and-cpap-machines
Free Case Evaluation
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