{"url_path":"/fda/device/recalls/Z-2948-2026","section_key":"summary","section_title":"DEVICE Recall: Cardinal Health 200, LLC — Cardinal Health Presource Kits:  1) KIT, MER NEURO BACK           , Catalog Number: PN33NBMYD;   2) KIT,CHP BASIC NEURO           , Catalog Number: PN36NBCH4;   3) KIT,CHP BASIC NEURO           , Catalog Number: PN36NBCH5;   4) KIT, ANT CERVICAL DISC        , Catalog Number: PN41ACLA9;   5) KIT, ANT CERVICAL DISC        , Catalog Number: PN41ACLA9;   6) K…","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-2948-2026%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":2802,"has_tables":false,"body_markdown":null}