{"url_path":"/fda/device/recalls/Z-2160-2026","section_key":"summary","section_title":"DEVICE Recall: Bolton Medical Inc. — RelayPro Thoracic Stent-Graft System (various sizes)  Reference numbers: 28-N4-32-104-32U\t28-N4-32-164-28U\t28-N4-32-164-32U\t28-N4-32-209-28U\t28-N4-32-209-32U\t28-N4-32-259-32U\t28-N4-34-109-34U\t28-N4-34-154-30U\t28-N4-34-154-34U\t28-N4-34-209-30U\t28-N4-34-209-34U\t28-N4-34-259-34U\t28-N4-36-109-36U\t28-N4-36-154-32U\t28-N4-36-154-36U\t28-N4-36-199-32U\t28-N4-36-199-36U\t…","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-04-22","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2160-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"Bolton Medical Inc."},"word_count":284,"has_tables":false,"body_markdown":null}