{
  "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": "South Jordan",
      "state": "UT",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "64303",
      "recalling_firm": "Ultradent Products, Inc.",
      "address_1": "505 W 10200 S",
      "address_2": "N/A",
      "postal_code": "84095-3935",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "USA Nationwide Distribution including the states of CA, AZ, CO and WA.",
      "recall_number": "Z-0876-2013",
      "product_description": "Avex CX Suite, Avex CX 0.22 UL4,5 HK  REF #224-017,       Product Usage:  Avex CX ceramic brackets are formed with 99.9% pure alumina oxide. The indicated use of the Avex CX ceramic bracket is the mechanical movement of natural teeth in conjunction with other components designed to attach to the brackets.",
      "product_quantity": "124",
      "reason_for_recall": "Orthodontic brackets distributed was incorrectly labeled.",
      "recall_initiation_date": "20130208",
      "center_classification_date": "20130222",
      "termination_date": "20130607",
      "report_date": "20130306",
      "code_info": "Lot R131360"
    }
  ]
}