{"url_path":"/fda/device/recalls/Z-2016-2026","section_key":"summary","section_title":"DEVICE Recall: Medline Industries, LP — Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows:    1. OPEN HEART CDS PART A, Medline Kit Number/SKU CDS840402AI;   2. OPEN HEART CDS, Medline Kit Number/SKU CDS984890V;   3. RR-NEURO VASCULAR PACK-LF, Medline Kit Number/SKU DYNJ0394874L;   4. VP SHUNT PACK-LF, Medline Kit Number/SKU DYNJ0750993M;   5. PEDI VP SHUNT ADD …","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-2016-2026%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":2412,"has_tables":false,"body_markdown":null}