{"data":{"matter":{"matter_id":"mat_cb5ea01cbb3b2a","slug":"bard-powerport","name":"Bard PowerPort Catheter Fracture","category":"mass_tort","subcategory":"medical_device","status":"litigated","score":0.77,"score_30d":null,"velocity":null,"headline":"Bard PowerPort catheter fracture and migration claims","summary":"C.R. Bard implantable port catheters used for long-term IV chemotherapy delivery have been alleged to fracture and migrate into the bloodstream, causing blood clots, infection, and the need for emergency surgical retrieval. MDL No. 3081 consolidates cases in the District of Arizona. Bellwether trials scheduled 2025-2026.","eligibility_hint":"Had a Bard PowerPort or similar implantable port and experienced fracture, migration, or thrombosis","payout":{"band":"large","low_cents":500000,"high_cents":15000000,"low_usd":5000,"high_usd":150000},"keywords":{"products":["powerport","implantable port","catheter"],"brands":["bard","becton dickinson","bd"]},"links":{"primary":"https://www.azd.uscourts.gov/mdl-3081","self":"https://getclaimscout.com/api/v1/matters/bard-powerport","html":"https://getclaimscout.com/matters/bard-powerport","lp":null},"lifecycle":{"first_seen_iso":"2026-05-19T11:12:27Z","last_signal_iso":"2026-06-22T22:04:45Z","mdl_filed_iso":null,"settlement_announced_iso":null,"claims_open_iso":null,"claims_close_iso":null,"narrative_generated_iso":"2026-06-22T22:04:45Z"},"attached_cases_count":0,"embedding_model":null,"embedding_version":1,"schema_version":1},"attached_cases":[],"recent_signals":[{"signal_id":"sig_a6af22cca1c77f","matter_id":"mat_cb5ea01cbb3b2a","source":"google_news","source_id":"gnews:CBMiekFVX3lxTFBPNVVFaGYyZjg5YzBGUkRIakdObmNaU0h2MzNWRWljWkthTGlWZVB4c2Jvbnh6cHk4U0QtcmZzTkxlWWluNk11Mlg5alRhZ1Rja0dWZVdvMDlmUTlFRk1nMHp1TE42MjNSZ0Q2Q2l3OG1HZFJjaWtCaGxR","kind":"news_article","title":"Bard PowerPort Lawsuit - Lawsuit Information Center","summary":"Bard PowerPort Lawsuit    Lawsuit Information Center","url":"https://news.google.com/rss/articles/CBMiekFVX3lxTFBPNVVFaGYyZjg5YzBGUkRIakdObmNaU0h2MzNWRWljWkthTGlWZVB4c2Jvbnh6cHk4U0QtcmZzTkxlWWluNk11Mlg5alRhZ1Rja0dWZVdvMDlmUTlFRk1nMHp1TE42MjNSZ0Q2Q2l3OG1HZFJjaWtCaGxR?oc=5","score":0.55,"decayed_score":null,"keywords":{"brands":["bard","becton dickinson","bd"],"products":["powerport","implantable port","catheter"]},"provenance":{"feed":"google_news_rss","published":"Wed, 17 Jun 2026 07:00:00 GMT","source_url":"https://news.google.com/rss/articles/CBMiekFVX3lxTFBPNVVFaGYyZjg5YzBGUkRIakdObmNaU0h2MzNWRWljWkthTGlWZVB4c2Jvbnh6cHk4U0QtcmZzTkxlWWluNk11Mlg5alRhZ1Rja0dWZVdvMDlmUTlFRk1nMHp1TE42MjNSZ0Q2Q2l3OG1HZFJjaWtCaGxR?oc=5","retrieved_at":"2026-07-04T08:35:59Z","search_query":"\"powerport\" (lawsuit OR settlement OR recall OR \"class action\")"},"resolved_by":"auto","resolution_confidence":0.9625,"first_seen_iso":"2026-06-16T11:10:00Z","last_seen_iso":"2026-07-04T08:35:59Z","schema_version":1},{"signal_id":"sig_d438ec8e5f4ef4","matter_id":"mat_cb5ea01cbb3b2a","source":"courtlistener_search","source_id":"cl-search:69696310","kind":"court_filing","title":"CL filing: White v. 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(BASD) -3006260740","retrieved_at":"2026-07-04T08:37:52Z"},"resolved_by":"auto","resolution_confidence":0.775,"first_seen_iso":"2026-06-09T09:44:45Z","last_seen_iso":"2026-07-04T08:37:52Z","schema_version":1},{"signal_id":"sig_27a8673be6223d","matter_id":"mat_cb5ea01cbb3b2a","source":"fda_maude","source_id":"maude:3006260740-2026-03692","kind":"device_adverse_event","title":"MAUDE: POWERPORT CLEARVUE ISP IMPLANTABLE PORT, CHRONOFLEX SINGLE-LUMEN, 8F — Device Appears to Trigger Rejection; Obstruction of Flow","summary":"FDA MAUDE Report 3006260740-2026-03692. Device: POWERPORT CLEARVUE ISP IMPLANTABLE PORT, CHRONOFLEX SINGLE-LUMEN, 8F (PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR). Manufacturer: C.R. BARD, INC. (BASD) -3006260740. Event type: Injury. Problems: Device Appears to Trigger Rejection; Obstruction of Flow.","url":"https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/detail.cfm?mdrfoi__id=3006260740-2026-03692","score":0.7,"decayed_score":null,"keywords":{"brands":["bard","becton dickinson","bd"],"products":["powerport","implantable port","catheter"]},"provenance":{"feed":"fda_openfda_maude","received":"20260528","report_no":"3006260740-2026-03692","brand_name":"POWERPORT CLEARVUE ISP IMPLANTABLE PORT, CHRONOFLEX SINGLE-LUMEN, 8F","event_type":"Injury","source_url":"https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/detail.cfm?mdrfoi__id=3006260740-2026-03692","device_query":"powerport","manufacturer":"C.R. BARD, INC. (BASD) -3006260740","retrieved_at":"2026-07-04T08:37:52Z"},"resolved_by":"auto","resolution_confidence":0.7375,"first_seen_iso":"2026-06-09T09:44:45Z","last_seen_iso":"2026-07-04T08:37:52Z","schema_version":1},{"signal_id":"sig_9eccf044685e6a","matter_id":"mat_cb5ea01cbb3b2a","source":"fda_maude","source_id":"maude:3006260740-2026-03690","kind":"device_adverse_event","title":"MAUDE: POWERPORT ISP M.R.I. IMPLANTABLE PORT, CHRONOFLEX SINGLE-LUMEN, 8F — Adverse Event Without Identified Device or Use Problem","summary":"FDA MAUDE Report 3006260740-2026-03690. Device: POWERPORT ISP M.R.I. IMPLANTABLE PORT, CHRONOFLEX SINGLE-LUMEN, 8F (PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR). Manufacturer: C.R. BARD, INC. (BASD) -3006260740. Event type: Injury. 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