{"url_path":"/fda/device/recalls/Z-1827-2026","section_key":"summary","section_title":"DEVICE Recall: WHILL, INC. — WHILL Model F, with software versions before HMI: 2.23 / MC: 1.05; the device is an indoor/outdoor, foldable battery-operated 2-wheel drive (rear-wheel   drive) powered wheelchair.","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2025-12-29","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1827-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"WHILL, INC."},"word_count":2109,"has_tables":false,"body_markdown":null}