{"url_path":"/fda/device/recalls/Z-2036-2026","section_key":"summary","section_title":"DEVICE Recall: Medline Industries, LP — Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows:   1. ANTERIOR CERVICAL FUSION PACK, Medline Kit Number/SKU DYNJ40566C;   2. OB PACK (OBSJD)642-LF, Medline Kit Number/SKU DYNJ47491F;   3. ANTERIOR CERVICAL-LF, Medline Kit Number/SKU DYNJ58274;   4. ANTERIOR CERVICAL-LF, Medline Kit Number/SKU DYNJ58344;   5. ANTERIOR CER…","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-03-19","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2036-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"Medline Industries, LP"},"word_count":745,"has_tables":false,"body_markdown":null}