{"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":0.6404,"velocity":-0.0125,"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":"2026-10-15T11:15:46Z","mdl_filed_iso":null,"settlement_announced_iso":null,"claims_open_iso":null,"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_1eabe848d00279","matter_id":"mat_cb5ea01cbb3b2a","source":"google_news","source_id":"gnews:CBMipgFBVV95cUxPQ2xBMjZ6a3N1ZmYtNTlYSVAzZm9VTml1czExMVZhUGJadlhlM05UemtZRjFEYmNLYjN5NWVCNE1YUjdPN2s3LU9OcVBRNU80MDhpNXl6RDJfdEJDdnZwakJCbmxTOU5IcFdYNzlDRVVtVDJINmVFSzN1RjJvc3BGckQ1XzYyeUM3aWxOM1U3N2RHb2RkWk9qNTBDSXFPb2s4ajdPYUFR","kind":"news_article","title":"Fourth Bard PowerPort Bellwether Case Set for Trial Dec. 1, as Third Gets Underway - AboutLawsuits.com","summary":"Fourth Bard PowerPort Bellwether Case Set for Trial Dec. 1, as Third Gets Underway    AboutLawsuits.com","url":"https://news.google.com/rss/articles/CBMipgFBVV95cUxPQ2xBMjZ6a3N1ZmYtNTlYSVAzZm9VTml1czExMVZhUGJadlhlM05UemtZRjFEYmNLYjN5NWVCNE1YUjdPN2s3LU9OcVBRNU80MDhpNXl6RDJfdEJDdnZwakJCbmxTOU5IcFdYNzlDRVVtVDJINmVFSzN1RjJvc3BGckQ1XzYyeUM3aWxOM1U3N2RHb2RkWk9qNTBDSXFPb2s4ajdPYUFR?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, 14 Oct 2026 15:00:00 GMT","source_url":"https://news.google.com/rss/articles/CBMipgFBVV95cUxPQ2xBMjZ6a3N1ZmYtNTlYSVAzZm9VTml1czExMVZhUGJadlhlM05UemtZRjFEYmNLYjN5NWVCNE1YUjdPN2s3LU9OcVBRNU80MDhpNXl6RDJfdEJDdnZwakJCbmxTOU5IcFdYNzlDRVVtVDJINmVFSzN1RjJvc3BGckQ1XzYyeUM3aWxOM1U3N2RHb2RkWk9qNTBDSXFPb2s4ajdPYUFR?oc=5","retrieved_at":"2026-10-18T10:49:35Z","search_query":"\"powerport\" (lawsuit OR settlement OR recall OR \"class action\")"},"resolved_by":"auto","resolution_confidence":0.9625,"first_seen_iso":"2026-10-15T11:15:46Z","last_seen_iso":"2026-10-18T10:49:35Z","schema_version":1},{"signal_id":"sig_4bac4cfb5aa435","matter_id":"mat_cb5ea01cbb3b2a","source":"fda_maude","source_id":"maude:50944847","kind":"device_adverse_event","title":"MAUDE: PowerPort ClearVUE — Difficult to Flush","summary":"FDA MAUDE Report 50944847. Device: PowerPort ClearVUE (PORT  CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR). Manufacturer: Bard Access Systems, Inc.. Event type: Malfunction. Problems: Difficult to Flush.","url":"https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/detail.cfm?mdrfoi__id=50944847","score":0.55,"decayed_score":null,"keywords":{"brands":["bard","becton dickinson","bd"],"products":["powerport","implantable port","catheter"]},"provenance":{"feed":"fda_openfda_maude","received":"20260930","report_no":"50944847","brand_name":"PowerPort ClearVUE","event_type":"Malfunction","source_url":"https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/detail.cfm?mdrfoi__id=50944847","device_query":"powerport","manufacturer":"Bard Access Systems, Inc.","retrieved_at":"2026-10-18T10:51:50Z"},"resolved_by":"auto","resolution_confidence":0.6,"first_seen_iso":"2026-10-13T14:02:17Z","last_seen_iso":"2026-10-18T10:51:50Z","schema_version":1},{"signal_id":"sig_17f1a390a681bc","matter_id":"mat_cb5ea01cbb3b2a","source":"fda_maude","source_id":"maude:3006260740-2026-07092","kind":"device_adverse_event","title":"MAUDE: PowerPort Slim Implantable Port, ChronoFlex Single-Lumen, 6F — Material Integrity Problem","summary":"FDA MAUDE Report 3006260740-2026-07092. Device: PowerPort Slim Implantable Port, ChronoFlex Single-Lumen, 6F (Port & Catheter, Implanted, Subcutaneous, Intravascular). Manufacturer: C.R. Bard, Inc. (BASD) -3006260740. Event type: Malfunction. Problems: Material Integrity Problem.","url":"https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/detail.cfm?mdrfoi__id=3006260740-2026-07092","score":0.55,"decayed_score":null,"keywords":{"brands":["bard","becton dickinson","bd"],"products":["powerport","implantable port","catheter"]},"provenance":{"feed":"fda_openfda_maude","received":"20260930","report_no":"3006260740-2026-07092","brand_name":"PowerPort Slim Implantable Port, ChronoFlex Single-Lumen, 6F","event_type":"Malfunction","source_url":"https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/detail.cfm?mdrfoi__id=3006260740-2026-07092","device_query":"powerport","manufacturer":"C.R. Bard, Inc. (BASD) -3006260740","retrieved_at":"2026-10-18T10:51:50Z"},"resolved_by":"auto","resolution_confidence":0.7375,"first_seen_iso":"2026-10-13T14:02:17Z","last_seen_iso":"2026-10-18T10:51:50Z","schema_version":1},{"signal_id":"sig_2a56ce3568bc57","matter_id":"mat_cb5ea01cbb3b2a","source":"fda_maude","source_id":"maude:3006260740-2026-07091","kind":"device_adverse_event","title":"MAUDE: PowerPort Slim Ti w 6Fr ChronoFlex wo SP, Inter. Kit — Device Appears to Trigger Rejection","summary":"FDA MAUDE Report 3006260740-2026-07091. Device: PowerPort Slim Ti w 6Fr ChronoFlex wo SP, Inter. Kit (Port & Catheter, Implanted, Subcutaneous, Intravascular). Manufacturer: C.R. Bard, Inc. (BASD) -3006260740. Event type: Injury. Problems: Device Appears to Trigger Rejection.","url":"https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/detail.cfm?mdrfoi__id=3006260740-2026-07091","score":0.7,"decayed_score":null,"keywords":{"brands":["bard","becton dickinson","bd"],"products":["powerport","implantable port","catheter"]},"provenance":{"feed":"fda_openfda_maude","received":"20260930","report_no":"3006260740-2026-07091","brand_name":"PowerPort Slim Ti w 6Fr ChronoFlex wo SP, Inter. Kit","event_type":"Injury","source_url":"https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/detail.cfm?mdrfoi__id=3006260740-2026-07091","device_query":"powerport","manufacturer":"C.R. Bard, Inc. (BASD) -3006260740","retrieved_at":"2026-10-18T10:51:50Z"},"resolved_by":"auto","resolution_confidence":0.6,"first_seen_iso":"2026-10-13T14:02:17Z","last_seen_iso":"2026-10-18T10:51:50Z","schema_version":1},{"signal_id":"sig_831f2ef7243437","matter_id":"mat_cb5ea01cbb3b2a","source":"fda_maude","source_id":"maude:3006260740-2026-07096","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 3006260740-2026-07096. 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=3006260740-2026-07096","score":0.7,"decayed_score":null,"keywords":{"brands":["bard","becton dickinson","bd"],"products":["powerport","implantable port","catheter"]},"provenance":{"feed":"fda_openfda_maude","received":"20260930","report_no":"3006260740-2026-07096","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=3006260740-2026-07096","device_query":"powerport","manufacturer":"C.R. Bard, Inc. 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