{"data":{"matter":{"matter_id":"mat_6bfea401f25fcb","slug":"philips-cpap","name":"Philips CPAP / BiPAP Recall","category":"mass_tort","subcategory":"medical_device","status":"claims_open","score":0.95,"score_30d":0.7173,"velocity":-0.0854,"headline":"Philips CPAP/BiPAP recall - personal injury and economic loss claims open","summary":"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.","eligibility_hint":"Used a recalled Philips DreamStation, BiPAP, Trilogy or System One device between 2009 and June 2021","payout":{"band":"large","low_cents":50000,"high_cents":10000000,"low_usd":500,"high_usd":100000},"keywords":{"products":["dreamstation","cpap","bipap","trilogy","respironics"],"brands":["philips","respironics"]},"links":{"primary":"https://www.usa.philips.com/healthcare/medical-alert/important-information","self":"https://www.getclaimscout.com/api/v1/matters/philips-cpap","html":"https://www.getclaimscout.com/matters/philips-cpap","lp":null},"lifecycle":{"first_seen_iso":"2026-05-19T11:12:26Z","last_signal_iso":"2026-07-14T08:05:25Z","mdl_filed_iso":null,"settlement_announced_iso":null,"claims_open_iso":"2024-09-01","claims_close_iso":null,"narrative_generated_iso":"2026-07-07T10:06:25Z"},"attached_cases_count":0,"embedding_model":null,"embedding_version":1,"schema_version":1},"attached_cases":[],"recent_signals":[{"signal_id":"sig_706ace3ebeac57","matter_id":"mat_6bfea401f25fcb","source":"fda_maude","source_id":"maude:2518422-2026-027437","kind":"device_adverse_event","title":"MAUDE: DREAMSTATION AUTO CPAP — Degraded","summary":"FDA MAUDE Report 2518422-2026-027437. 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Problems: Degraded.","url":"https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/detail.cfm?mdrfoi__id=2518422-2026-027385","score":0.55,"decayed_score":null,"keywords":{"brands":["philips","respironics"],"products":["dreamstation","cpap","bipap","trilogy","respironics"]},"provenance":{"feed":"fda_openfda_maude","received":"20260630","report_no":"2518422-2026-027385","brand_name":"DREAMSTATION AUTO CPAP","event_type":"Malfunction","source_url":"https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/detail.cfm?mdrfoi__id=2518422-2026-027385","device_query":"dreamstation","manufacturer":"RESPIRONICS, INC.","retrieved_at":"2026-07-16T08:14:08Z"},"resolved_by":"auto","resolution_confidence":0.5175,"first_seen_iso":"2026-07-14T08:05:25Z","last_seen_iso":"2026-07-16T08:14:08Z","schema_version":1},{"signal_id":"sig_ab0aff2874dc7d","matter_id":"mat_6bfea401f25fcb","source":"fda_maude","source_id":"maude:2518422-2026-027397","kind":"device_adverse_event","title":"MAUDE: DREAMSTATION AUTO CPAP — Degraded","summary":"FDA MAUDE Report 2518422-2026-027397. 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