{"url_path":"/fda/device/recalls/Z-2945-2026","section_key":"summary","section_title":"DEVICE Recall: Cardinal Health 200, LLC — Cardinal Health Presource Kits: 1) ENT TRAY                      , Catalog Number: 24-0726A;  2) KIT,SINUS                     , Catalog Number: PE13SPAJA;  3) KIT,SINUS                     , Catalog Number: PE13SPAJB;  4) KIT, SINUS                    , Catalog Number: PE13SPAJC;  5) KIT,NASAL SEPTOPLASTY,F, Catalog Number: PE13SPAJC;  6) KIT,NASAL SEPTO…","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-07-14","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2945-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"Cardinal Health 200, LLC"},"word_count":2795,"has_tables":false,"body_markdown":null}