{"url_path":"/fda/device/recalls/Z-2805-2026","section_key":"summary","section_title":"DEVICE Recall: Permobil Inc — M5 Corpus Power Wheelchair  REF,120032","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2025-06-19","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2805-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"Permobil Inc"},"word_count":134,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2805-2026\n\n**Recalling firm:** Permobil Inc\n**Classification:** Class II\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2025-06-19\n**Report date:** 2026-08-05\n\n## Product\nM5 Corpus Power Wheelchair  REF,120032\n\n## Reason\nThis recall is being reported retroactively. Power Platform firmware is missing specific drive inhibit logic. This issue may allow the chair to drive under restricted conditions, and may create an unstable condition in certain circumstances.\n\n## Affected lots\nPower Platform firmware versions 1.27 through 1.57 UDI-DI 17330818334562\n\n## Distribution\nWorldwide - US: Nationwide distribution in the states of AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KY, ME, MI, MN, MO, MS, MT, NC, ND, NJ, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, VT, WA, WI, WV, WY and the country of CANADA."}