{
  "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": "2026-08-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "102837",
      "product_res_number": "Z-0187-2012",
      "event_date_initiated": "2011-06-23",
      "event_date_posted": "2011-11-14",
      "recall_status": "Terminated",
      "event_date_terminated": "2013-07-02",
      "res_event_number": "59461",
      "product_code": "LLI",
      "product_description": "Invacare  600 lb. Bariatric Bed, Head motor extension cable used on component numbers BAR5490 and BAR5490IVC.  These components are part of the following Bed Model Number(s): BAR600, BARPKGCA, BAR600IVC, BARPKGIVC-1633, and BARPKG.",
      "code_info": "Model Number(s): BAR600, BARPKGCA, BAR600IVC, BARPKGIVC-1633, and BARPKG.  35747 serial numbers available from Invacare.",
      "firm_fei_number": "1525712",
      "recalling_firm": "Invacare Corporation",
      "address_1": "1200 Taylor St",
      "city": "Elyria",
      "state": "OH",
      "postal_code": "44035-6248",
      "additional_info_contact": "440-329-6595",
      "reason_for_recall": "Invacare Corporation decided to recall the products because risk analysis reveals that miskeying or disconnection of the head motor extension cable during bed set-up may result in product damage, or in rare instances, the potential for fire.",
      "root_cause_description": "Labeling design",
      "action": "On 9/19/11, Invacare sent Recall Notificaiton Letters to their customers. They instructed their customers to quarantine the product, complete and return a response form.",
      "product_quantity": "35,747",
      "distribution_pattern": "Distribution Nationwide and to United Arab Emirates, Dominican Republic, Egypt, Guam, Mexico, & Virgin Islands.",
      "openfda": {
        "k_number": [
          "K840787",
          "K022387"
        ],
        "registration_number": [
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        "device_name": "Bed, Therapeutic, Ac-Powered, Adjustable Home-Use",
        "medical_specialty_description": "General Hospital",
        "regulation_number": "880.5100",
        "device_class": "2"
      }
    }
  ]
}