{"recall":{"id":"fda-device-99315","source":"FDA","sourceName":"U.S. Food and Drug Administration (openFDA device enforcement)","cat":"medicines","kids":false,"kind":"device","title":"Permobil Inc recalls Permobil M3 Corpus Power Wheelchair with Heavy Duty Shock REF:120031","firm":"Permobil Inc","date":"2024-02-29","reported":"2026-08-05","status":"Ongoing","classification":"Class II","products":[{"name":"Permobil M3 Corpus Power Wheelchair with Heavy Duty Shock REF:120031, Model version 3","code":"All Units operating with firmware version 1.26.2/UDI:(01)17330818345674","quantity":"140 units","number":"Z-2795-2026","classification":"Class II"}],"reason":"This 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,","hazard":"FDA Class II: may cause temporary or medically reversible adverse health consequences (FDA definition).","affected":"Worldwide - 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.","nationwide":true,"states":[],"units":"140 units","remedy":"","whatToDo":"Check your product against the names and codes above. The FDA enforcement record lists the recall as voluntary: firm initiated; it does not state a consumer remedy, so follow the firm’s notice or the FDA link.","contact":"","url":"https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99315","apiUrl":"https://api.fda.gov/device/enforcement.json?search=report_date:[20260705+TO+20991231]&sort=report_date:desc&limit=1000","rawHash":"08a5dc8548df8cac","firstSeen":"2026-11-02T13:57:14.206Z","updatedAt":"2026-11-02T13:57:14.206Z","history":[]},"official":{"fetchedAt":"2026-11-02T13:57:14.206Z","apiUrl":"https://api.fda.gov/device/enforcement.json?search=report_date:[20260705+TO+20991231]&sort=report_date:desc&limit=1000","officialUrl":"https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99315","record":[{"status":"Ongoing","city":"Lebanon","state":"TN","country":"United States","classification":"Class II","openfda":{},"product_type":"Devices","event_id":"99315","recalling_firm":"Permobil Inc","address_1":"300 Duke Dr","address_2":"N/A","postal_code":"37090-8115","voluntary_mandated":"Voluntary: Firm initiated","initial_firm_notification":"Letter","distribution_pattern":"Worldwide - 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.","recall_number":"Z-2795-2026","product_description":"Permobil M3 Corpus Power Wheelchair with Heavy Duty Shock  REF:120031, Model version 3","product_quantity":"140 units","reason_for_recall":"This 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,","recall_initiation_date":"20240229","center_classification_date":"20260724","report_date":"20260805","code_info":"All Units operating with firmware version 1.26.2/UDI:(01)17330818345674"}]}}