{
  "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": "2026-08-13",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "30393",
      "product_res_number": "Z-0206-04",
      "event_date_initiated": "2003-11-14",
      "event_date_posted": "2003-12-10",
      "recall_status": "Terminated",
      "event_date_terminated": "2004-08-06",
      "res_event_number": "27711",
      "product_code": "KMM",
      "product_description": "Hill-Rom brand Resident LT bed ambulatory assist bar accessory; accessory P865A.",
      "code_info": "All units distributed between March 1997 and September 2003.",
      "firm_fei_number": "1824206",
      "recalling_firm": "Hill-Rom, Inc.",
      "address_1": "125 E Pearl St",
      "city": "Batesville",
      "state": "IN",
      "postal_code": "47006",
      "additional_info_contact": "800-445-3720",
      "reason_for_recall": "The ambulatory assist bar may not lock into position and may come out of place due to incorrect assembly.",
      "root_cause_description": "Other",
      "action": "Customers were advised of the recall by letter dated 11/12/03 and mailed on 11/14/03.  A Hill-Rom representative will visit each customer to assure the latching mechanism is properly attached to the bed.",
      "product_quantity": "1400",
      "distribution_pattern": "United States and Canada",
      "openfda": {}
    }
  ]
}