{"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":0.7684,"velocity":-0.1997,"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://www.getclaimscout.com/api/v1/matters/bard-powerport","html":"https://www.getclaimscout.com/matters/bard-powerport","lp":null},"lifecycle":{"first_seen_iso":"2026-05-19T11:12:27Z","last_signal_iso":"2026-07-14T08:05:30Z","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_e2e59448d15650","matter_id":"mat_cb5ea01cbb3b2a","source":"fda_maude","source_id":"maude:3006260740-2026-04562","kind":"device_adverse_event","title":"MAUDE: POWERPORT CLEARVUE ISP IMPLANTABLE PORT, CHRONOFLEX SINGLE-LUMEN, 8F — Migration","summary":"FDA MAUDE Report 3006260740-2026-04562. Device: POWERPORT CLEARVUE ISP IMPLANTABLE PORT, CHRONOFLEX SINGLE-LUMEN, 8F (PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR). Manufacturer: C.R. BARD, INC. (BASD) -3006260740. Event type: Malfunction. Problems: Migration.","url":"https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/detail.cfm?mdrfoi__id=3006260740-2026-04562","score":0.55,"decayed_score":null,"keywords":{"brands":["bard","becton dickinson","bd"],"products":["powerport","implantable port","catheter"]},"provenance":{"feed":"fda_openfda_maude","received":"20260630","report_no":"3006260740-2026-04562","brand_name":"POWERPORT CLEARVUE ISP IMPLANTABLE PORT, CHRONOFLEX SINGLE-LUMEN, 8F","event_type":"Malfunction","source_url":"https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/detail.cfm?mdrfoi__id=3006260740-2026-04562","device_query":"powerport","manufacturer":"C.R. BARD, INC. (BASD) -3006260740","retrieved_at":"2026-07-16T08:14:12Z"},"resolved_by":"auto","resolution_confidence":0.7375,"first_seen_iso":"2026-07-14T08:05:30Z","last_seen_iso":"2026-07-16T08:14:12Z","schema_version":1},{"signal_id":"sig_fe76ff9ab0ad97","matter_id":"mat_cb5ea01cbb3b2a","source":"fda_maude","source_id":"maude:3006260740-2026-04556","kind":"device_adverse_event","title":"MAUDE: POWERPORT CLEARVUE ISP — Adverse Event Without Identified Device or Use Problem","summary":"FDA MAUDE Report 3006260740-2026-04556. Device: POWERPORT CLEARVUE ISP (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=3006260740-2026-04556","score":0.7,"decayed_score":null,"keywords":{"brands":["bard","becton dickinson","bd"],"products":["powerport","implantable port","catheter"]},"provenance":{"feed":"fda_openfda_maude","received":"20260630","report_no":"3006260740-2026-04556","brand_name":"POWERPORT CLEARVUE ISP","event_type":"Injury","source_url":"https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/detail.cfm?mdrfoi__id=3006260740-2026-04556","device_query":"powerport","manufacturer":"C.R. BARD, INC. (BASD) -3006260740","retrieved_at":"2026-07-16T08:14:12Z"},"resolved_by":"auto","resolution_confidence":0.6,"first_seen_iso":"2026-07-14T08:05:30Z","last_seen_iso":"2026-07-16T08:14:12Z","schema_version":1},{"signal_id":"sig_ef375c53a9efd1","matter_id":"mat_cb5ea01cbb3b2a","source":"fda_maude","source_id":"maude:3006260740-2026-04557","kind":"device_adverse_event","title":"MAUDE: POWERPORT ISP M.R.I. IMPLANTABLE PORT, CHRONOFLEX SINGLE-LUMEN, 8F — Device Appears to Trigger Rejection","summary":"FDA MAUDE Report 3006260740-2026-04557. 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. Problems: Device Appears to Trigger Rejection.","url":"https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/detail.cfm?mdrfoi__id=3006260740-2026-04557","score":0.7,"decayed_score":null,"keywords":{"brands":["bard","becton dickinson","bd"],"products":["powerport","implantable port","catheter"]},"provenance":{"feed":"fda_openfda_maude","received":"20260630","report_no":"3006260740-2026-04557","brand_name":"POWERPORT ISP M.R.I. IMPLANTABLE PORT, CHRONOFLEX SINGLE-LUMEN, 8F","event_type":"Injury","source_url":"https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/detail.cfm?mdrfoi__id=3006260740-2026-04557","device_query":"powerport","manufacturer":"C.R. BARD, INC. (BASD) -3006260740","retrieved_at":"2026-07-16T08:14:12Z"},"resolved_by":"auto","resolution_confidence":0.7375,"first_seen_iso":"2026-07-14T08:05:30Z","last_seen_iso":"2026-07-16T08:14:12Z","schema_version":1},{"signal_id":"sig_ef62f483f24056","matter_id":"mat_cb5ea01cbb3b2a","source":"fda_maude","source_id":"maude:3006260740-2026-04559","kind":"device_adverse_event","title":"MAUDE: POWERPORT ISP M.R.I. IMPLANTABLE PORT, GROSHONG SINGLE-LUMEN, 8F — Adverse Event Without Identified Device or Use Problem","summary":"FDA MAUDE Report 3006260740-2026-04559. Device: POWERPORT ISP M.R.I. IMPLANTABLE PORT, GROSHONG 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=3006260740-2026-04559","score":0.7,"decayed_score":null,"keywords":{"brands":["bard","becton dickinson","bd"],"products":["powerport","implantable port","catheter"]},"provenance":{"feed":"fda_openfda_maude","received":"20260630","report_no":"3006260740-2026-04559","brand_name":"POWERPORT ISP M.R.I. IMPLANTABLE PORT, GROSHONG SINGLE-LUMEN, 8F","event_type":"Injury","source_url":"https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/detail.cfm?mdrfoi__id=3006260740-2026-04559","device_query":"powerport","manufacturer":"C.R. BARD, INC. (BASD) -3006260740","retrieved_at":"2026-07-16T08:14:12Z"},"resolved_by":"auto","resolution_confidence":0.7375,"first_seen_iso":"2026-07-14T08:05:30Z","last_seen_iso":"2026-07-16T08:14:12Z","schema_version":1},{"signal_id":"sig_317737bede9372","matter_id":"mat_cb5ea01cbb3b2a","source":"fda_maude","source_id":"maude:3006260740-2026-04560","kind":"device_adverse_event","title":"MAUDE: POWERPORT ISP M.R.I. IMPLANTABLE PORT, CHRONOFLEX SINGLE-LUMEN, 8F — Device Appears to Trigger Rejection","summary":"FDA MAUDE Report 3006260740-2026-04560. 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. Problems: Device Appears to Trigger Rejection.","url":"https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/detail.cfm?mdrfoi__id=3006260740-2026-04560","score":0.7,"decayed_score":null,"keywords":{"brands":["bard","becton dickinson","bd"],"products":["powerport","implantable port","catheter"]},"provenance":{"feed":"fda_openfda_maude","received":"20260630","report_no":"3006260740-2026-04560","brand_name":"POWERPORT ISP M.R.I. IMPLANTABLE PORT, CHRONOFLEX SINGLE-LUMEN, 8F","event_type":"Injury","source_url":"https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/detail.cfm?mdrfoi__id=3006260740-2026-04560","device_query":"powerport","manufacturer":"C.R. BARD, INC. (BASD) -3006260740","retrieved_at":"2026-07-16T08:14:12Z"},"resolved_by":"auto","resolution_confidence":0.7375,"first_seen_iso":"2026-07-14T08:05:30Z","last_seen_iso":"2026-07-16T08:14:12Z","schema_version":1},{"signal_id":"sig_9e95facecbfbf3","matter_id":"mat_cb5ea01cbb3b2a","source":"fda_maude","source_id":"maude:3006260740-2026-04561","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 3006260740-2026-04561. 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=3006260740-2026-04561","score":0.7,"decayed_score":null,"keywords":{"brands":["bard","becton dickinson","bd"],"products":["powerport","implantable port","catheter"]},"provenance":{"feed":"fda_openfda_maude","received":"20260630","report_no":"3006260740-2026-04561","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=3006260740-2026-04561","device_query":"powerport","manufacturer":"C.R. BARD, INC. (BASD) -3006260740","retrieved_at":"2026-07-16T08:14:12Z"},"resolved_by":"auto","resolution_confidence":0.7375,"first_seen_iso":"2026-07-14T08:05:30Z","last_seen_iso":"2026-07-16T08:14:12Z","schema_version":1},{"signal_id":"sig_a0f96d34fc1f33","matter_id":"mat_cb5ea01cbb3b2a","source":"google_news","source_id":"gnews:CBMiT0FVX3lxTFBwOExUWHZ4UGFkcVZKdEdqVElqdEpFWU1xeVhQaFowV01Ka2d1TEdrdGxuUGg0SWxrdDZFSktjRFVabnFhZ1dvbTBtMUQ1cUE","kind":"news_article","title":"PowerPort Lawsuit 2026: Payouts, Eligibility, Updates - LawFold.com","summary":"PowerPort Lawsuit 2026: Payouts, Eligibility, Updates &nbsp;&nbsp; LawFold.com","url":"https://news.google.com/rss/articles/CBMiT0FVX3lxTFBwOExUWHZ4UGFkcVZKdEdqVElqdEpFWU1xeVhQaFowV01Ka2d1TEdrdGxuUGg0SWxrdDZFSktjRFVabnFhZ1dvbTBtMUQ1cUE?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":"Tue, 23 Jun 2026 07:00:00 GMT","source_url":"https://news.google.com/rss/articles/CBMiT0FVX3lxTFBwOExUWHZ4UGFkcVZKdEdqVElqdEpFWU1xeVhQaFowV01Ka2d1TEdrdGxuUGg0SWxrdDZFSktjRFVabnFhZ1dvbTBtMUQ1cUE?oc=5","retrieved_at":"2026-07-10T09:33:48Z","search_query":"\"powerport\" (lawsuit OR settlement OR recall OR \"class action\")"},"resolved_by":"auto","resolution_confidence":0.9625,"first_seen_iso":"2026-07-10T09:33:48Z","last_seen_iso":"2026-07-10T09:33:48Z","schema_version":1},{"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 &nbsp;&nbsp; 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":"2026-07-16T08:12:01Z","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":"2026-07-16T08:12:01Z","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. AngioDynamics, Inc.","summary":"Federal filing in ohnd, docket 1:25-cv-00407, dated 2025-03-01.","url":"https://www.courtlistener.com/recap/?q=powerport","score":0.75,"decayed_score":null,"keywords":{"brands":[],"products":[]},"provenance":{"feed":"courtlistener_v4_search","court":"ohnd","docket_no":"1:25-cv-00407","date_filed":"2025-03-01","source_url":"https://www.courtlistener.com/recap/?q=powerport","retrieved_at":"2026-07-16T08:19:48Z","search_query":"powerport"},"resolved_by":"search_context","resolution_confidence":0.3,"first_seen_iso":"2026-06-11T10:30:12Z","last_seen_iso":"2026-07-16T08:19:48Z","schema_version":1},{"signal_id":"sig_adb1fe79951246","matter_id":"mat_cb5ea01cbb3b2a","source":"google_news","source_id":"gnews:CBMirwFBVV95cUxPcmx1OWJabHVaOGlhbTJ6SmtqOEhUMVYzT2xxN1BCZHRLTWc3SlZWMkphZ1VoYjNUWmxjZ3RBU2RMeGdRWHlPdGRWb05qRzVBZ2dGZGl4bFVsRlBJZ0c5Z0JzV2dmU0lGSkNYSG5MSnc2eG5OVzBkVUV6TjRhdkUtT0d5ZXV3OGFjdW1sT0FWRDJfWWdzZ2pMekRxMDFBV2Y0Y214dmZTVWQ0SlQ4dTRR","kind":"news_article","title":"Final Pretrial Conference in Bard PowerPort Lawsuit To Be Held April 9 - AboutLawsuits.com","summary":"Final Pretrial Conference in Bard PowerPort Lawsuit To Be Held April 9 &nbsp;&nbsp; AboutLawsuits.com","url":"https://news.google.com/rss/articles/CBMirwFBVV95cUxPcmx1OWJabHVaOGlhbTJ6SmtqOEhUMVYzT2xxN1BCZHRLTWc3SlZWMkphZ1VoYjNUWmxjZ3RBU2RMeGdRWHlPdGRWb05qRzVBZ2dGZGl4bFVsRlBJZ0c5Z0JzV2dmU0lGSkNYSG5MSnc2eG5OVzBkVUV6TjRhdkUtT0d5ZXV3OGFjdW1sT0FWRDJfWWdzZ2pMekRxMDFBV2Y0Y214dmZTVWQ0SlQ4dTRR?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":"Fri, 27 Mar 2026 07:00:00 GMT","source_url":"https://news.google.com/rss/articles/CBMirwFBVV95cUxPcmx1OWJabHVaOGlhbTJ6SmtqOEhUMVYzT2xxN1BCZHRLTWc3SlZWMkphZ1VoYjNUWmxjZ3RBU2RMeGdRWHlPdGRWb05qRzVBZ2dGZGl4bFVsRlBJZ0c5Z0JzV2dmU0lGSkNYSG5MSnc2eG5OVzBkVUV6TjRhdkUtT0d5ZXV3OGFjdW1sT0FWRDJfWWdzZ2pMekRxMDFBV2Y0Y214dmZTVWQ0SlQ4dTRR?oc=5","retrieved_at":"2026-06-15T12:13:10Z","search_query":"\"powerport\" (lawsuit OR settlement OR recall OR \"class action\")"},"resolved_by":"auto","resolution_confidence":0.9625,"first_seen_iso":"2026-06-10T09:59:17Z","last_seen_iso":"2026-06-15T12:13:10Z","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":"2026-07-13T09:27:31Z"},"resolved_by":"auto","resolution_confidence":0.7375,"first_seen_iso":"2026-06-09T09:44:45Z","last_seen_iso":"2026-07-13T09:27:31Z","schema_version":1},{"signal_id":"sig_4db1a33d85a93f","matter_id":"mat_cb5ea01cbb3b2a","source":"fda_maude","source_id":"maude:3006260740-2026-03694","kind":"device_adverse_event","title":"MAUDE: POWERPORT ISP IMPLANTABLE PORT, GROSHONG, 8F — Fracture","summary":"FDA MAUDE Report 3006260740-2026-03694. Device: POWERPORT ISP IMPLANTABLE PORT, GROSHONG, 8F (PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR). Manufacturer: C.R. BARD, INC. (BASD) -3006260740. Event type: Malfunction. Problems: Fracture.","url":"https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/detail.cfm?mdrfoi__id=3006260740-2026-03694","score":0.55,"decayed_score":null,"keywords":{"brands":["bard","becton dickinson","bd"],"products":["powerport","implantable port","catheter"]},"provenance":{"feed":"fda_openfda_maude","received":"20260528","report_no":"3006260740-2026-03694","brand_name":"POWERPORT ISP IMPLANTABLE PORT, GROSHONG, 8F","event_type":"Malfunction","source_url":"https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/detail.cfm?mdrfoi__id=3006260740-2026-03694","device_query":"powerport","manufacturer":"C.R. BARD, INC. (BASD) -3006260740","retrieved_at":"2026-07-13T09:27:31Z"},"resolved_by":"auto","resolution_confidence":0.775,"first_seen_iso":"2026-06-09T09:44:45Z","last_seen_iso":"2026-07-13T09:27:31Z","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. Problems: Adverse Event Without Identified Device or Use Problem.","url":"https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/detail.cfm?mdrfoi__id=3006260740-2026-03690","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":"3006260740-2026-03690","brand_name":"POWERPORT ISP M.R.I. IMPLANTABLE PORT, CHRONOFLEX SINGLE-LUMEN, 8F","event_type":"Injury","source_url":"https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/detail.cfm?mdrfoi__id=3006260740-2026-03690","device_query":"powerport","manufacturer":"C.R. BARD, INC. (BASD) -3006260740","retrieved_at":"2026-07-13T09:27:31Z"},"resolved_by":"auto","resolution_confidence":0.7375,"first_seen_iso":"2026-06-09T09:44:44Z","last_seen_iso":"2026-07-13T09:27:31Z","schema_version":1},{"signal_id":"sig_1c27259eed24e7","matter_id":"mat_cb5ea01cbb3b2a","source":"fda_maude","source_id":"maude:3006260740-2026-03691","kind":"device_adverse_event","title":"MAUDE: POWERPORT M.R.I. IMPLANTABLE PORT, SILICONE SINGLE-LUMEN, KIT, 9.6F — Expulsion","summary":"FDA MAUDE Report 3006260740-2026-03691. Device: POWERPORT M.R.I. IMPLANTABLE PORT, SILICONE SINGLE-LUMEN, KIT, 9.6F (PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR). Manufacturer: C.R. BARD, INC. (BASD) -3006260740. Event type: Injury. Problems: Expulsion.","url":"https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/detail.cfm?mdrfoi__id=3006260740-2026-03691","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":"3006260740-2026-03691","brand_name":"POWERPORT M.R.I. IMPLANTABLE PORT, SILICONE SINGLE-LUMEN, KIT, 9.6F","event_type":"Injury","source_url":"https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/detail.cfm?mdrfoi__id=3006260740-2026-03691","device_query":"powerport","manufacturer":"C.R. BARD, INC. (BASD) -3006260740","retrieved_at":"2026-07-13T09:27:31Z"},"resolved_by":"auto","resolution_confidence":0.7375,"first_seen_iso":"2026-06-09T09:44:44Z","last_seen_iso":"2026-07-13T09:27:31Z","schema_version":1},{"signal_id":"sig_3330f72ceb185f","matter_id":"mat_cb5ea01cbb3b2a","source":"fda_maude","source_id":"maude:3006260740-2026-03693","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 3006260740-2026-03693. 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=3006260740-2026-03693","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":"3006260740-2026-03693","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=3006260740-2026-03693","device_query":"powerport","manufacturer":"C.R. BARD, INC. (BASD) -3006260740","retrieved_at":"2026-07-13T09:27:31Z"},"resolved_by":"auto","resolution_confidence":0.7375,"first_seen_iso":"2026-06-09T09:44:44Z","last_seen_iso":"2026-07-13T09:27:31Z","schema_version":1},{"signal_id":"sig_1b6ca1bf58b0ca","matter_id":"mat_cb5ea01cbb3b2a","source":"fda_maude","source_id":"maude:3006260740-2026-03689","kind":"device_adverse_event","title":"MAUDE: POWERPORT CLEARVUE ISP IMPLANTABLE PORT, CHRONOFLEX SINGLE-LUMEN, 8F — Device Appears to Trigger Rejection","summary":"FDA MAUDE Report 3006260740-2026-03689. 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.","url":"https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/detail.cfm?mdrfoi__id=3006260740-2026-03689","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":"3006260740-2026-03689","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=3006260740-2026-03689","device_query":"powerport","manufacturer":"C.R. BARD, INC. (BASD) -3006260740","retrieved_at":"2026-07-13T09:27:31Z"},"resolved_by":"auto","resolution_confidence":0.7375,"first_seen_iso":"2026-06-09T09:44:44Z","last_seen_iso":"2026-07-13T09:27:31Z","schema_version":1},{"signal_id":"sig_a4238005482003","matter_id":"mat_cb5ea01cbb3b2a","source":"courtlistener_search","source_id":"cl-search:71774144","kind":"court_filing","title":"CL filing: MEDICAL COMPONENTS, INC. v. BECTON DICKINSON AND COMPANY","summary":"Federal filing in njd, docket 2:25-cv-16949, dated 2025-10-27.","url":"https://www.courtlistener.com/recap/?q=powerport","score":0.75,"decayed_score":null,"keywords":{"brands":[],"products":[]},"provenance":{"feed":"courtlistener_v4_search","court":"njd","docket_no":"2:25-cv-16949","date_filed":"2025-10-27","source_url":"https://www.courtlistener.com/recap/?q=powerport","retrieved_at":"2026-07-16T08:19:47Z","search_query":"powerport"},"resolved_by":"search_context","resolution_confidence":0.3,"first_seen_iso":"2026-06-07T09:04:10Z","last_seen_iso":"2026-07-16T08:19:47Z","schema_version":1},{"signal_id":"sig_9b5e661ddf866b","matter_id":"mat_cb5ea01cbb3b2a","source":"courtlistener_search","source_id":"cl-search:69674040","kind":"court_filing","title":"CL filing: Sanchez v. Becton Dickinson and Company","summary":"Federal filing in azd, docket 2:25-cv-00487, dated 2025-02-13.","url":"https://www.courtlistener.com/recap/?q=powerport","score":0.75,"decayed_score":null,"keywords":{"brands":[],"products":[]},"provenance":{"feed":"courtlistener_v4_search","court":"azd","docket_no":"2:25-cv-00487","date_filed":"2025-02-13","source_url":"https://www.courtlistener.com/recap/?q=powerport","retrieved_at":"2026-07-16T08:19:48Z","search_query":"powerport"},"resolved_by":"search_context","resolution_confidence":0.3,"first_seen_iso":"2026-06-07T09:04:10Z","last_seen_iso":"2026-07-16T08:19:48Z","schema_version":1},{"signal_id":"sig_b46462bb15a462","matter_id":"mat_cb5ea01cbb3b2a","source":"courtlistener_search","source_id":"cl-search:69578039","kind":"court_filing","title":"CL filing: Levidiotis v. Becton Dickinson and Company","summary":"Federal filing in azd, docket 2:25-cv-00213, dated 2025-01-23.","url":"https://www.courtlistener.com/recap/?q=powerport","score":0.75,"decayed_score":null,"keywords":{"brands":[],"products":[]},"provenance":{"feed":"courtlistener_v4_search","court":"azd","docket_no":"2:25-cv-00213","date_filed":"2025-01-23","source_url":"https://www.courtlistener.com/recap/?q=powerport","retrieved_at":"2026-07-16T08:19:48Z","search_query":"powerport"},"resolved_by":"search_context","resolution_confidence":0.3,"first_seen_iso":"2026-06-07T09:04:10Z","last_seen_iso":"2026-07-16T08:19:48Z","schema_version":1},{"signal_id":"sig_2b108bb4792a38","matter_id":"mat_cb5ea01cbb3b2a","source":"courtlistener_search","source_id":"cl-search:69551863","kind":"court_filing","title":"CL filing: CogniPower LLC v. Fantasia Trading LLC","summary":"Federal filing in ded, docket 1:25-cv-00066, dated 2025-01-16.","url":"https://www.courtlistener.com/recap/?q=powerport","score":0.75,"decayed_score":null,"keywords":{"brands":[],"products":[]},"provenance":{"feed":"courtlistener_v4_search","court":"ded","docket_no":"1:25-cv-00066","date_filed":"2025-01-16","source_url":"https://www.courtlistener.com/recap/?q=powerport","retrieved_at":"2026-07-16T08:19:48Z","search_query":"powerport"},"resolved_by":"search_context","resolution_confidence":0.3,"first_seen_iso":"2026-06-07T09:04:10Z","last_seen_iso":"2026-07-16T08:19:48Z","schema_version":1},{"signal_id":"sig_951fdbde96c427","matter_id":"mat_cb5ea01cbb3b2a","source":"courtlistener_search","source_id":"cl-search:69537548","kind":"court_filing","title":"CL filing: Ogbolu v. Becton Dickinson and Company","summary":"Federal filing in azd, docket 2:25-cv-00068, dated 2025-01-10.","url":"https://www.courtlistener.com/recap/?q=powerport","score":0.75,"decayed_score":null,"keywords":{"brands":[],"products":[]},"provenance":{"feed":"courtlistener_v4_search","court":"azd","docket_no":"2:25-cv-00068","date_filed":"2025-01-10","source_url":"https://www.courtlistener.com/recap/?q=powerport","retrieved_at":"2026-07-16T08:19:48Z","search_query":"powerport"},"resolved_by":"search_context","resolution_confidence":0.3,"first_seen_iso":"2026-06-07T09:04:10Z","last_seen_iso":"2026-07-16T08:19:48Z","schema_version":1},{"signal_id":"sig_7ec023f988c030","matter_id":"mat_cb5ea01cbb3b2a","source":"courtlistener_search","source_id":"cl-search:69537546","kind":"court_filing","title":"CL filing: Menchan v. Becton Dickinson and Company","summary":"Federal filing in azd, docket 2:25-cv-00077, dated 2025-01-10.","url":"https://www.courtlistener.com/recap/?q=powerport","score":0.75,"decayed_score":null,"keywords":{"brands":[],"products":[]},"provenance":{"feed":"courtlistener_v4_search","court":"azd","docket_no":"2:25-cv-00077","date_filed":"2025-01-10","source_url":"https://www.courtlistener.com/recap/?q=powerport","retrieved_at":"2026-06-10T10:06:57Z","search_query":"powerport"},"resolved_by":"search_context","resolution_confidence":0.3,"first_seen_iso":"2026-06-07T09:04:10Z","last_seen_iso":"2026-06-10T10:06:57Z","schema_version":1},{"signal_id":"sig_d37daa1030d203","matter_id":"mat_cb5ea01cbb3b2a","source":"courtlistener_search","source_id":"cl-search:71686853","kind":"court_filing","title":"CL filing: Taylor v. Becton Dickinson and Company","summary":"Federal filing in azd, docket 2:25-cv-03652, dated 2025-10-02.","url":"https://www.courtlistener.com/recap/?q=powerport","score":0.75,"decayed_score":null,"keywords":{"brands":[],"products":[]},"provenance":{"feed":"courtlistener_v4_search","court":"azd","docket_no":"2:25-cv-03652","date_filed":"2025-10-02","source_url":"https://www.courtlistener.com/recap/?q=powerport","retrieved_at":"2026-07-16T08:19:48Z","search_query":"powerport"},"resolved_by":"search_context","resolution_confidence":0.3,"first_seen_iso":"2026-06-07T09:04:10Z","last_seen_iso":"2026-07-16T08:19:48Z","schema_version":1},{"signal_id":"sig_40447b64fd4790","matter_id":"mat_cb5ea01cbb3b2a","source":"courtlistener_search","source_id":"cl-search:69537565","kind":"court_filing","title":"CL filing: Taylor v. Becton Dickinson and Company","summary":"Federal filing in azd, docket 2:25-cv-00080, dated 2025-01-10.","url":"https://www.courtlistener.com/recap/?q=powerport","score":0.75,"decayed_score":null,"keywords":{"brands":[],"products":[]},"provenance":{"feed":"courtlistener_v4_search","court":"azd","docket_no":"2:25-cv-00080","date_filed":"2025-01-10","source_url":"https://www.courtlistener.com/recap/?q=powerport","retrieved_at":"2026-07-16T08:19:48Z","search_query":"powerport"},"resolved_by":"search_context","resolution_confidence":0.3,"first_seen_iso":"2026-06-07T09:04:10Z","last_seen_iso":"2026-07-16T08:19:48Z","schema_version":1},{"signal_id":"sig_9b5c8a5ea24abe","matter_id":"mat_cb5ea01cbb3b2a","source":"courtlistener_search","source_id":"cl-search:69578015","kind":"court_filing","title":"CL filing: Tucker v. Becton Dickinson and Company","summary":"Federal filing in azd, docket 2:25-cv-00181, dated 2025-01-22.","url":"https://www.courtlistener.com/recap/?q=powerport","score":0.75,"decayed_score":null,"keywords":{"brands":[],"products":[]},"provenance":{"feed":"courtlistener_v4_search","court":"azd","docket_no":"2:25-cv-00181","date_filed":"2025-01-22","source_url":"https://www.courtlistener.com/recap/?q=powerport","retrieved_at":"2026-07-16T08:19:48Z","search_query":"powerport"},"resolved_by":"search_context","resolution_confidence":0.3,"first_seen_iso":"2026-06-07T09:04:10Z","last_seen_iso":"2026-07-16T08:19:48Z","schema_version":1}]},"meta":{"api_version":"v1","schema_version":1,"self":"https://www.getclaimscout.com/api/v1/matters/bard-powerport","docs":"https://getclaimscout.com/openapi.json","llms_txt":"https://getclaimscout.com/llms.txt"}}