{"url_path":"/fda/device/recalls/Z-2037-2026","section_key":"summary","section_title":"DEVICE Recall: Medline Industries, LP — Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows:   1. CATARACT PACK, Medline Kit Number/SKU DYNJ48725A;   2. OCULAR PACK, Medline Kit Number/SKU DYNJ64138B;   3. OCULOPLASTY PACK, Medline Kit Number/SKU DYNJ64572A;   4. OCULOPLASTY PACK, Medline Kit Number/SKU DYNJ64572B;   5. MICROSURGERY PACK, Medline Kit Number/SKU DY…","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-2037-2026%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":1364,"has_tables":false,"body_markdown":null}