{"url_path":"/fda/device/recalls/Z-1948-2026","section_key":"summary","section_title":"DEVICE Recall: Medtronic, Inc. — Medtronic Sphere-9 Catheter, Model Number AFR-00001; catheter, percutaneous, cardiac ablation, for treatment of atrial flutter.","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-03-11","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1948-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"Medtronic, Inc."},"word_count":2334,"has_tables":false,"body_markdown":null}