Philips CPAP / BiPAP Recall
Claims open now
Large payouts ($5k-$50k)
mass_tort · medical_device
Philips CPAP/BiPAP recall - personal injury and economic loss claims open
Eligibility hint
Used a recalled Philips DreamStation, BiPAP, Trilogy or System One device between 2009 and June 2021
Philips recalled approximately 15 million CPAP, BiPAP and ventilator devices in 2021 over a PE-PUR sound-abatement foam defect that could release particulate matter and toxic chemicals into the airway. Personal injury settlements and an economic loss settlement are both active. Users with documented use between 2009 and June 2021 may be eligible for refund, replacement, or injury compensation.
Recent signals
- MAUDE: DREAMSTATION — Degraded
- MAUDE: DREAMSTATION — Degraded
- MAUDE: DREAMSTATION — Degraded
- MAUDE: DREAMSTATION — Degraded
- MAUDE: DREAMSTATION — Degraded
- MAUDE: DREAMSTATION — Degraded
- Philip Feucht - Exemption/Rulemaking
- Letter from EPA to Verdant Law, April 3, 2023
- Petition for Administrative Reconsideration and Stay submitted by Verdant Law, March 18, 2025
- Harber, Philip, and William S. Beckett. "Health effects of filtering facepiece respirators: Research and clinical implications of comfort, thermal, skin, psychologic, and workplace effects." American Journal of Industrial Medicine 66.12 (2023): 1017-1032.
Brands:
philipsrespironics
Products: dreamstationcpapbipaptrilogyrespironics
Products: dreamstationcpapbipaptrilogyrespironics
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