Philips CPAP and BiPAP Recall Lawsuit: Injury Claims & Legal Updates
What is Philips CPAP and BiPAP Recall Lawsuit?
The Philips CPAP and BiPAP recall lawsuit involves thousands of patients who used recalled Philips CPAP machines, BiPAP machines, and ventilators that allegedly exposed them to toxic foam particles and harmful chemical gases.
If you or a loved one used a recalled Philips CPAP machine and later developed respiratory problems, cancer, or other injuries, you may be eligible to file a claim and seek compensation.
The Philips CPAP and BiPAP recall lawsuit centers on allegations that Philips knowingly sold defective sleep apnea devices containing sound-abatement foam that could break down and release dangerous particles and toxic chemicals into users’ airways.
Thousands of personal injury claims have been consolidated into a federal multidistrict litigation (MDL). Plaintiffs seek compensation for medical expenses, lost wages, pain and suffering, and long-term health monitoring.
Philips has agreed to a $1.1 billion settlement in the US to resolve all pending lawsuits, providing compensation to affected individuals for medical costs and other damages
Explain Philips CPAP and BiPAP Recall
CPAP and BiPAP devices are used to help patients maintain proper airflow and oxygen levels during sleep.
In June 2021, Philips announced a massive recall of millions of Philips CPAP, BiPAP, and ventilator devices due to defective polyester-based polyurethane (PE-PUR) foam. This foam was intended to reduce noise but was found to:
Break down into inhalable particles
Release toxic and potentially carcinogenic gases
Degrade faster when exposed to heat, humidity, or ozone cleaners
The recall affected patients across the U.S. who relied on these devices nightly to treat sleep apnea and respiratory conditions.
Who is Eligible to File a Claim?
You may be eligible to file a Philips CPAP recall lawsuit if:
You used a recalled Philips CPAP machine or BiPAP machine
You experienced respiratory symptoms, organ damage, or cancer after use
You required medical treatment linked to foam exposure
You still possess proof of device use or medical diagnosis
Both patients and families of deceased users may qualify for compensation.
Philips CPAP/BiPAP Health Risks: Foam Degradation & Associated Injuries
Philips' CPAP and BiPAP devices have been linked to several serious health risks due to the breakdown of the sound-dampening foam. Many users have reported ongoing discomfort, breathing problems, and other complications because of exposure to the defective material.
Major health risks associated with Philips CPAP and BiPAP
Skin Irritation
Foam particles can cause rashes, redness, and irritation around the face and airways.
Carcinogenic Risk
Some chemicals in the degraded foam are suspected to be carcinogenic, increasing long-term cancer risk.
Respiratory Infections
Inhaled particles can lead to lung infections and other respiratory complications.
Asthma
Exposure to foam debris may trigger or worsen asthma symptoms in susceptible individuals.
Inflammatory Response
The body may react to inhaled particles with inflammation in the lungs and airways.
Headaches and Dizziness
Users may experience chronic headaches, dizziness, and related symptoms due to exposure to toxic chemicals.
Devices Affected by the Philips Recall: CPAP, BiPAP & Ventilators
The recall covers numerous Philips sleep and respiratory devices made between 2009 and April 26, 2001, and this includes:
A-Series BiPAP A30
A-Series BiPAP A40 (ventilator)
A-Series BiPAP Hybrid A30
A-Series BiPAP V30 Auto (ventilator)
C-Series ASV (ventilator)
C-Series S/T and AVAPS
DreamStation
DreamStation ASV
DreamStation Go
DreamStation ST, AVAPS
Dorma 400
Dorma 500
E30
Garbin Plus, Aeris, LifeVent (ventilator)
OmniLab Advanced+
REMstar SE Auto
SystemOne ASV4
SystemOne (Q-Series)
Trilogy 100 (ventilator)
Trilogy 200 (ventilator)
Philips also recalled certain Trilogy Evo ventilators that were distributed from April 15, 2021, to May 24, 2021, with specific serial numbers.
Philips CPAP and BiPAP Recall Lawsuit Update: Current Legal Developments
As of January 2026, 621 injury-related cases involving recalled Philips CPAP machines remain pending in the federal multidistrict litigation, and in December 2025, 680 lawsuits involving sleep apnea devices remain pending in MDL No. 3014.
On April 29, 2024, Philips Respironics agreed to a $1.1 billion settlement to resolve CPAP-related lawsuits. Approximately $1.075 billion of the settlement is allocated to personal injury claims involving serious health complications or deaths allegedly caused by the devices. An additional $25 million is designated for medical monitoring of individuals who used the recalled machines and may face future health risks. The settlement is still subject to approval by a federal court.
Previously, in early September 2023, Philips proposed a separate $479 million settlement to resolve CPAP class-action lawsuits related to recalled devices. That agreement does not affect the ongoing federal MDL proceedings.
How a Philips CPAP and BiPAP Recall Lawyer Can Help?
An experienced Philips CPAP recall attorney can:
Confirm whether your Philips CPAP machine qualifies
Collect medical records and device documentation
File claims within legal deadlines
Negotiate higher settlement payouts
Represent you in federal court if necessary
Compensation & Settlements in Philips CPAP/BiPAP Cases
Individuals affected by defective Philips CPAP and BiPAP devices may be entitled to financial compensation for the injuries and losses they have suffered. The company has established a $1.1 billion settlement fund to address health-related claims in the US.
Potential compensation include:
Unit-Based Claims
Eligible users may receive between $55 and $1,552 per recalled device, depending on device type and use.
Injury-Related Claims
Compensation will be distributed based on the severity and extent of medical injuries.
Medical Expenses
Covers costs for treatments, hospital visits, medications, and device replacements.
Pain and Suffering
Damages for physical discomfort, emotional distress, and reduced quality of life.
Future Medical Costs
Financial support for anticipated ongoing care related to device-related health issues.
How to File a Philips CPAP and BiPAP Lawsuit with Connect2Attorney?
Connect2Attorney guides you through the process of filing a Philips CPAP and BiPAP lawsuit against the responsible party, in just three simple steps:
Submit a Free Case Review
Share details about your situation so we can understand your claim.
Confirm Eligibility
Our legal team will review your case and let you know if you qualify.
Sign Agreement
If eligible, sign a legal agreement. Your attorney will handle all legal formalities.
Philips CPAP and BiPAP Lawsuit Lawsuit Timeline
2026First Half
January
As of January 2026, 621 injury-related lawsuits involving recalled Philips CPAP machines remain pending in the multidistrict litigation.
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What is the Philips CPAP and BiPAP recall about?
The Philips CPAP and BiPAP recall involves certain devices that contained polyester-based polyurethane (PE-PUR) foam, which could break down over time and release harmful particles or toxic chemicals into the air pathway.
Who is eligible to file a Philips CPAP lawsuit?
Individuals who used a recalled Philips CPAP, BiPAP, or ventilator device and later experienced respiratory problems, cancer, or other health complications may be eligible to file a lawsuit.
What health problems are linked to recalled Philips CPAP devices?
Reported health problems include respiratory irritation, inflammation, asthma flare-ups, chronic cough, headaches, dizziness, organ damage, and in some cases, cancer linked to toxic foam exposure.
How much compensation can I receive from a Philips CPAP lawsuit?
Compensation varies based on injury severity, medical expenses, and long-term health impact. Philips has set aside over $1.1 billion for settlements, and individual payouts may range from thousands to significant amounts depending on each case.
Do I need proof of injury to file a Philips CPAP lawsuit?
Yes. Medical records, proof of device use, diagnosis reports, and physician documentation linking your health condition to the recalled Philips device can help support your claim.
