{"url_path":"/fda/device/recalls/Z-2451-2026","section_key":"summary","section_title":"DEVICE Recall: Medtronic Navigation, Inc.-Boxborough — Medtronic O-arm O2 Imaging System. Model Number: BI70002000.","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-05-19","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2451-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"Medtronic Navigation, Inc.-Boxborough"},"word_count":784,"has_tables":false,"body_markdown":null}