{"url_path":"/fda/device/recalls/Z-2486-2026","section_key":"summary","section_title":"DEVICE Recall: Medline Industries, LP — MEDLINE Medical Procedure Kits labeled as:    1) BASIC HEART PACK, Medline Kit/SKU DYNJ67331B;   2) CARDIAC SURGERY, Medline Kit/SKU DYNJ911589A;   3) CAROTID ENDARTECOMY, Medline Kit/SKU DYNJ36211D;   4) CHLA ECMO / CARDIAC PACK, Medline Kit/SKU DYNJ87973;   5) CHLA ECMO / CARDIAC PACK, Medline Kit/SKU DYNJ87973A;   6) CV PART 1 AND 2, Medline Kit/SKU DYNJ…","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-05-04","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2486-2026%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":1277,"has_tables":false,"body_markdown":null}