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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. 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