{
  "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": "26284",
      "product_res_number": "Z-0671-03",
      "event_date_initiated": "2003-01-01",
      "event_date_posted": "2003-03-21",
      "recall_status": "Terminated",
      "event_date_terminated": "2008-06-25",
      "res_event_number": "25692",
      "product_code": "I--TI",
      "k_numbers": [
        "K991658"
      ],
      "product_description": "Permobil Chairman 2K powered wheelchair, Model 1280",
      "code_info": "Serial Numbers:  1100068 to 1103702",
      "firm_fei_number": "1221084",
      "recalling_firm": "Permobile Inc.",
      "address_1": "6961 Eastgate Blvd",
      "city": "Lebanon",
      "state": "TN",
      "postal_code": "370906005",
      "additional_info_contact": "Barry Steelman\n800-736-0925",
      "reason_for_recall": "Incidents were reported where a drive wheel has come off its motor axle, due either to loosening of the wheel bolt or a broken wheel bolt.",
      "root_cause_description": "Other",
      "action": "Permobil Inc has notified its field representatives of the voluntary recall and these representatives have been provided with lists of each Chairman 2K serial number and the Dealer to which the wheelchair was sold.",
      "product_quantity": "1582",
      "distribution_pattern": "Nationwide, Puerto Rico, Canada",
      "openfda": {}
    }
  ]
}