{"url_path":"/fda/device/recalls/Z-2811-2026","section_key":"summary","section_title":"DEVICE Recall: Medtronic Perfusion Systems — EOPA 3D Arterial Cannula 22FR, intended for use with cardiopulmonary bypass as an arterial return cannula, Model Number 78322","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-06-24","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2811-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"Medtronic Perfusion Systems"},"word_count":100,"has_tables":false,"body_markdown":null}