{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Noblesville",
      "state": "IN",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "66185",
      "recalling_firm": "King Systems Corp.",
      "address_1": "15011 Herriman Blvd",
      "address_2": "N/A",
      "postal_code": "46060-4253",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "Distributed in NY.",
      "recall_number": "Z-2255-2013",
      "product_description": "King LT-D Oropharyngeal Airways    The King LT-D is intended for use in adult patients (in excess of 25 kg) for controlled ventilation during anesthesia for procedures that are short in duration and when the patient is considered to have a low risk of aspiration of stomach contents.",
      "product_quantity": "9 cases; 45 products",
      "reason_for_recall": "Report that size 5 KLTD airways were packaged in pouches indicating a size of 2.5 and shipped to your facility. The correct size of the KLTD airway is clearly marked on the actual airway product and the physical size difference between 2.5 and 5 is distinct and obvious.",
      "recall_initiation_date": "20130903",
      "center_classification_date": "20130919",
      "termination_date": "20140415",
      "report_date": "20130925",
      "code_info": "Part Number KLTD2125  Lot Number I10RG",
      "more_code_info": ""
    }
  ]
}