{"url_path":"/fda/device/recalls/Z-2795-2026","section_key":"summary","section_title":"DEVICE Recall: Permobil Inc — Permobil M3 Corpus Power Wheelchair with Heavy Duty Shock  REF:120031, Model version 3","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2024-02-29","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2795-2026%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":145,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2795-2026\n\n**Recalling firm:** Permobil Inc\n**Classification:** Class II\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2024-02-29\n**Report date:** 2026-08-05\n\n## Product\nPermobil M3 Corpus Power Wheelchair with Heavy Duty Shock  REF:120031, Model version 3\n\n## Reason\nThis recall has been reported retroactively. The power wheelchair firmware lacks a speed restriction to maintain stability when the seat lift exceeds 50 mm, which may cause the user to fall from the wheelchair or the wheelchair to tip over,\n\n## Affected lots\nAll Units operating with firmware version 1.26.2/UDI:(01)17330818345674\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 CAN."}