{"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"},"lifecycle":{"first_seen_iso":"2026-05-19T11:12:27Z","last_signal_iso":"2026-05-19T11:12:27Z","mdl_filed_iso":null,"settlement_announced_iso":null,"claims_open_iso":null,"claims_close_iso":null,"narrative_generated_iso":"2026-05-19T11:12:27Z"},"attached_cases_count":0,"embedding_model":null,"embedding_version":1,"schema_version":1},"attached_cases":[],"recent_signals":[{"signal_id":"sig_d2912d2776c457","matter_id":"mat_cb5ea01cbb3b2a","source":"fda_maude","source_id":"maude:3006260740-2026-03005","kind":"device_adverse_event","title":"MAUDE: POWERPORT CLEARVUE SLIM IMPLANTABLE PORT, CHRONOFLEX SINGLE-LUMEN, KIT, 8F — Adverse Event Without Identified Device or Use Problem","summary":"FDA MAUDE Report 3006260740-2026-03005. Device: POWERPORT CLEARVUE SLIM IMPLANTABLE PORT, CHRONOFLEX SINGLE-LUMEN, KIT, 8F (PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR). Manufacturer: C.R. BARD, INC. (BASD) -3006260740. Event type: Injury. Problems: Adverse Event Without Identified Device or Use Problem.","url":"https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/detail.cfm?mdrfoi__id=3006260740-2026-03005","score":0.7,"decayed_score":null,"keywords":{"brands":["bard","becton dickinson","bd"],"products":["powerport","implantable port","catheter"]},"provenance":{"feed":"fda_openfda_maude","received":"20260430","report_no":"3006260740-2026-03005","brand_name":"POWERPORT CLEARVUE SLIM IMPLANTABLE PORT, CHRONOFLEX SINGLE-LUMEN, KIT, 8F","event_type":"Injury","source_url":"https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/detail.cfm?mdrfoi__id=3006260740-2026-03005","device_query":"powerport","manufacturer":"C.R. BARD, INC. 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Problems: Adverse Event Without Identified Device or Use Problem.","url":"https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/detail.cfm?mdrfoi__id=3006260740-2026-03006","score":0.7,"decayed_score":null,"keywords":{"brands":["bard","becton dickinson","bd"],"products":["powerport","implantable port","catheter"]},"provenance":{"feed":"fda_openfda_maude","received":"20260430","report_no":"3006260740-2026-03006","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=3006260740-2026-03006","device_query":"powerport","manufacturer":"C.R. BARD, INC. (BASD) -3006260740","retrieved_at":"2026-05-19T23:02:26Z"},"resolved_by":"auto","resolution_confidence":0.9625,"first_seen_iso":"2026-05-19T23:02:26Z","last_seen_iso":"2026-05-19T23:02:26Z","schema_version":1},{"signal_id":"sig_3c2c7742da3360","matter_id":"mat_cb5ea01cbb3b2a","source":"fda_maude","source_id":"maude:3006260740-2026-03003","kind":"device_adverse_event","title":"MAUDE: POWERPORT CLEARVUE ISP IMPLANTABLE PORT, CHRONOFLEX SINGLE-LUMEN, 8F — Adverse Event Without Identified Device or Use Problem","summary":"FDA MAUDE Report 3006260740-2026-03003. 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: Adverse Event Without Identified Device or Use Problem.","url":"https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/detail.cfm?mdrfoi__id=3006260740-2026-03003","score":0.7,"decayed_score":null,"keywords":{"brands":["bard","becton dickinson","bd"],"products":["powerport","implantable port","catheter"]},"provenance":{"feed":"fda_openfda_maude","received":"20260430","report_no":"3006260740-2026-03003","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=3006260740-2026-03003","device_query":"powerport","manufacturer":"C.R. BARD, INC. (BASD) -3006260740","retrieved_at":"2026-05-19T23:02:26Z"},"resolved_by":"auto","resolution_confidence":0.9625,"first_seen_iso":"2026-05-19T23:02:26Z","last_seen_iso":"2026-05-19T23:02:26Z","schema_version":1},{"signal_id":"sig_6ac38e01dae4bc","matter_id":"mat_cb5ea01cbb3b2a","source":"fda_maude","source_id":"maude:3006260740-2026-03011","kind":"device_adverse_event","title":"MAUDE: POWERPORT CLEARVUE ISP IMPLANTABLE PORT, CHRONOFLEX SINGLE-LUMEN, 8F — Adverse Event Without Identified Device or Use Problem","summary":"FDA MAUDE Report 3006260740-2026-03011. 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. 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(BASD) -3006260740","retrieved_at":"2026-05-19T23:02:26Z"},"resolved_by":"auto","resolution_confidence":0.9625,"first_seen_iso":"2026-05-19T23:02:26Z","last_seen_iso":"2026-05-19T23:02:26Z","schema_version":1},{"signal_id":"sig_c70c67aa33bb02","matter_id":"mat_cb5ea01cbb3b2a","source":"fda_maude","source_id":"maude:3006260740-2026-03007","kind":"device_adverse_event","title":"MAUDE: POWERPORT M.R.I. IMPLANTABLE PORT, CHRONOFLEX SINGLE-LUMEN, 8F — Adverse Event Without Identified Device or Use Problem","summary":"FDA MAUDE Report 3006260740-2026-03007. Device: POWERPORT 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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