{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "South Jordan",
      "address_1": "505 W 10200 S",
      "reason_for_recall": "Product was packaged into kits labeled as having a shelf life of 2103-05.  The correct shelf life is 2013-05.",
      "address_2": "",
      "product_quantity": "104 units",
      "code_info": "Lot B6LZS, Part number 5705",
      "center_classification_date": "20130326",
      "distribution_pattern": "USA: AL, CA, GA, IL, IN, MA, MD, MI, NJ, OK, PA, SC, UT; 12 International distributors: Germany, China, France, Spain",
      "state": "UT",
      "product_description": "Opalescence Treswhite Supreme Peach Patient Kit",
      "report_date": "20130403",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Ultradent Products, Inc.",
      "recall_number": "F-1271-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Food",
      "event_id": "64534",
      "termination_date": "20130709",
      "more_code_info": "",
      "recall_initiation_date": "20130308",
      "postal_code": "84095-3935",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}