Injury guide

CPAP Recall Symptoms: Care Questions and Records

Tell a clinician about your symptoms and the device you used. A symptom list cannot diagnose a foam injury.

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Updated Oct 4, 202611 sources

This may apply to you if

  • Identify the actual Philips model and your dates of use.
  • Bring the diagnosis and treatment records for an individual legal check.
  • Tell the lawyer about any replacement, earlier registration or agreement.

What the public record says

These are cited sources. Their inclusion does not imply that they endorse People’s Justice or reviewed this page.

Grégoire Justeau · Department of Respiratory and Sleep Medicine, Angers University Hospital, France · First-listed author of the original CPAP cancer cohort

Finding: The 4,447-person cohort found no increased overall cancer incidence among Philips users compared with other brands. Its observational design and follow-up cannot exclude every risk or decide an individual cause.

Justeau original CPAP cancer cohort, 2022 (opens in a new tab) · Jul 14, 2022 · Checked Oct 3, 2026

Joy Flowers Conti · United States District Court for the Western District of Pennsylvania · Senior United States District Judge

Finding: The January 16, 2026 opinion grants remand of the Graham case to Kentucky state court. It records past settlements and a January 31, 2025 private injury-settlement registration date; it does not decide personal medical cause or injury compensation.

Graham court opinion, January 16, 2026 (opens in a new tab) · Jan 16, 2026 · Checked Oct 3, 2026

The evidence and its limits

Pays de la Loire Sleep Cohort Study Group; Angers University Hospital, France · European Respiratory Journal · 2022

Cancer risk in adherent users of polyurethane foam-containing CPAP devices for sleep apnoea

Design:
Cohort
Participants:
4,447 patients, including 1,648 Philips and 2,799 other-device users
Finding:
No association with increased overall cancer incidence was found over a median 7.2-year follow-up.
Main limitation
Observational design, possible unmeasured factors and limited ability to detect certain cancers. Two authors disclosed Philips lecture honoraria outside the study. This does not establish individual cause or all-model safety.

Read the source: Cancer risk in adherent users of polyurethane foam-containing CPAP devices for sleep apnoea (opens in a new tab) · Checked Oct 3, 2026

The short answer

What is the health concern from recalled foam?
Foam in certain recalled Philips devices can break down. FDA describes potential health risks, not a diagnosis for each user. [6]
What signs should I discuss with a doctor?
Tell a doctor about headaches or trouble breathing. Explain when they started and which device you used. [6]
How are symptoms diagnosed and treated?
Ask a clinician what assessment and care fit your health. Discuss the risks of stopping, continuing or changing a recalled device. [6]
What does the evidence say about cancer fears?
FDA warns of possible risks from the foam. A French study found no higher overall cancer rate in Philips than other users. [8]

The process

What happens next

  1. 01

    You answer a few questions

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  2. 02

    A lawyer looks at it

    A lawyer at the firm reads your answers and checks them against the current case criteria.

  3. 03

    The firm decides and gets in touch

    If the firm takes your case, you get the terms in writing to read before you sign. You can always say no.

When it fits this case

  • Identify the actual Philips model and your dates of use.
  • Bring the diagnosis and treatment records for an individual legal check.
  • Tell the lawyer about any replacement, earlier registration or agreement.

Tell a clinician about your symptoms and the device you used. A symptom list cannot diagnose a foam injury. Talk about your care before you change how you use the device.

What is the health concern from recalled foam?

Foam in certain recalled Philips devices can break down. FDA describes potential health risks, not a diagnosis for each user.

The foam was used to reduce sound and vibration. Particles or some chemicals may reach the device’s air tubes and be breathed in or swallowed. A general risk warning does not establish that every symptom came from the machine; keep the actual device details for a medical assessment.

What signs should I discuss with a doctor?

Tell a doctor about headaches or trouble breathing. Explain when they started and which device you used.

FDA lists possible irritation of the airway and other areas, asthma, headaches and other potential effects. Share the full health history rather than treating this list as a diagnosis. Ask what needs assessment and whether a device problem should be reported; a report does not itself establish medical cause or compensation.

How are symptoms diagnosed and treated?

Ask a clinician what assessment and care fit your health. Discuss the risks of stopping, continuing or changing a recalled device.

FDA says some patients may face greater risk from stopping use than continuing. The provider can discuss the actual device and care alternatives. This page cannot choose a treatment or decide a test result; a product claim and a symptom complaint do not replace a personal clinical plan.

What does the evidence say about cancer fears?

FDA warns of possible risks from the foam. A French study found no higher overall cancer rate in Philips than other users.

The study included 4,447 patients and had a median 7.2-year follow-up. It was observational and may miss some cancer risks; two authors disclosed Philips lecture fees outside the work. Neither that finding nor a warning proves or excludes one person’s cancer cause, and no symptom here is a cancer diagnosis.

What safety steps and records should I keep?

Keep care notes, use dates, the model and serial number. Do not add a CPAP or BiPAP filter or remove its foam.

FDA advises against ozone or UV cleaners for these recalled machines and recommends talking with the provider about problems. Ask about covered health and billing copies and the exceptions to access. Before legal work, read the written fees and expenses and confirm the next step instead of assuming a record request files a claim.

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Sources

  1. HHS: Your Medical RecordsHHS: Your Medical Records · regulator
  2. Federal courts: civil casesFederal courts: civil cases · court
  3. ABA: fees paid from a successful claimABA: fees paid from a successful claim
  4. SDNY: filing time limitsSDNY: filing time limits · court
  5. ABA Model Rule 1.5: feesABA Model Rule 1.5: fees
  6. FDA recalled Philips device patient guidanceFDA recalled Philips device patient guidance · regulator
  7. FDA foam testing summaryFDA foam testing summary · regulator
  8. Justeau original CPAP cancer cohort, 2022Justeau original CPAP cancer cohort, 2022 · study
  9. Graham court opinion, January 16, 2026Graham court opinion, January 16, 2026 · court
  10. Philips announced (Apr 29, 2024) a $1.1 billion total resolution of US Respironics personal-injury and medical-monitoring litigation; the official court settlement site confirms $1.075 billion for personal-injury claims in MDL 3014 and Massachusetts state court (~58,000 registrants; injuries diagnosed by Apr 29, 2024 qualify). A January 16, 2026 court opinion says payments were anticipated in early 2026; no admission of liability.respironicspisettlement.com · Apr 29, 2024
  11. Philips announced resolution of the US economic-loss class litigation in MDL 3014 (Sept 7, 2023 press release): predefined cash awards by device type, extended warranties, and a return bonus; Philips' release cites a EUR 575 million Q1 2023 provision and explicitly excludes personal injury and medical monitoring claims. The commonly cited $479 million settlement figure is from secondary press coverage (Drugwatch), not Philips' own release — flagged accordingly.usa.philips.com · Sep 7, 2023

Checked against 9 primary sources by People's Justice editors · Updated

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