{"recall":{"id":"fda-device-99267","source":"FDA","sourceName":"U.S. Food and Drug Administration (openFDA device enforcement)","cat":"medicines","kids":false,"kind":"device","title":"Permobil Inc recalls M5 Corpus Power Wheelchair REF","firm":"Permobil Inc","date":"2025-06-19","reported":"2026-08-05","status":"Ongoing","classification":"Class II","products":[{"name":"M5 Corpus Power Wheelchair REF,120032","code":"Power Platform firmware versions 1.27 through 1.57 UDI-DI 17330818334562","quantity":"715 wheelchairs","number":"Z-2805-2026","classification":"Class II"}],"reason":"This 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.","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 CANADA.","nationwide":true,"states":[],"units":"715 wheelchairs","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=99267","apiUrl":"https://api.fda.gov/device/enforcement.json?search=report_date:[20260705+TO+20991231]&sort=report_date:desc&limit=1000","rawHash":"7f5c501cc7f5577e","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=99267","record":[{"status":"Ongoing","city":"Lebanon","state":"TN","country":"United States","classification":"Class II","openfda":{},"product_type":"Devices","event_id":"99267","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":"Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit","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 CANADA.","recall_number":"Z-2805-2026","product_description":"M5 Corpus Power Wheelchair  REF,120032","product_quantity":"715 wheelchairs","reason_for_recall":"This 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.","recall_initiation_date":"20250619","center_classification_date":"20260724","report_date":"20260805","code_info":"Power Platform firmware versions 1.27 through 1.57 UDI-DI 17330818334562"}]}}