{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-08-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "111792",
      "product_res_number": "Z-0557-2013",
      "event_date_initiated": "2012-08-06",
      "event_date_posted": "2012-12-18",
      "recall_status": "Terminated",
      "event_date_terminated": "2014-01-29",
      "res_event_number": "62826",
      "product_code": "ILK",
      "k_numbers": [
        "K121560"
      ],
      "product_description": "ThyssenKrupp Accessibility LEVANT Stairlift.\r\n\r\nIntended to mechanically transport one mobility impaired person in a fold-down seat up and down straight stairs, indoors and outdoors.",
      "code_info": "Stairlifts sold between 12/5/08-7/31/12. The product does not have lot numbers assigned and no expiration date.",
      "firm_fei_number": "1925312",
      "recalling_firm": "ThyssenKrupp Access Corp",
      "address_1": "4001 E 138th St",
      "city": "Grandview",
      "state": "MO",
      "postal_code": "64030-2837",
      "additional_info_contact": "Kevin L. Brinkman\n816-965-4712",
      "reason_for_recall": "The seat could break as a result of damage resulting from a seat belt being trapped underneath the foldable part of the seat when the seat belt is not buckled.",
      "root_cause_description": "Device Design",
      "action": "The firm, ThyssenKrupp Access sent an \"IMPORTANT SAFETY AND PRODUCT USE INFORMATION\" letter dated August 6, 2012 to all affected customers.  The letter identified the product, problem, and  actions to be taken by the customers.\r\nContact the firm at 1-800-925-3100 ext. 5484 for assistance regarding this recall.",
      "product_quantity": "5,413 stairlifts",
      "distribution_pattern": "Worldwide Distribution-USA (nationwide) including the states of  IL, IN, MI, OH, WI, IA, KS, MN, MO, NE, SD, AR, LA,OK, TX. AZ, CO, ID, MT, NM, UT, MT, AK, CA, HI, OR, WA, AL, FL, GA, KY, NC,  SC, TN, MD, PA, VA, WV, CT, MA, ME, NH, NJ, NY, RI and VT and the countries of  Canada, Nova Scotia and British Columbia",
      "openfda": {
        "k_number": [
          "K121560",
          "K864152",
          "K921648",
          "K023852",
          "K033829",
          "K890555",
          "K073110",
          "K850877",
          "K091858",
          "K121561",
          "K882091",
          "K240843",
          "K022509",
          "K862738",
          "K770294",
          "K103122",
          "K871582",
          "K970927",
          "K024167",
          "K803063",
          "K130864",
          "K113308",
          "K932625",
          "K896628",
          "K111858",
          "K864324",
          "K222818",
          "K024345",
          "K884110",
          "K033438",
          "K854461",
          "K032880",
          "K093946",
          "K882669",
          "K033752",
          "K923912"
        ],
        "registration_number": [
          "3008729900",
          "3005753836",
          "3008791629",
          "9615370",
          "1831750"
        ],
        "fei_number": [
          "3002807131",
          "3008729900",
          "3005753836",
          "3008791629",
          "1831750"
        ],
        "device_name": "Transport, Patient, Powered",
        "medical_specialty_description": "Physical Medicine",
        "regulation_number": "890.5150",
        "device_class": "2"
      }
    }
  ]
}