{
  "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": [
    {
      "status": "Terminated",
      "city": "Atlanta",
      "state": "GA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Food",
      "event_id": "73831",
      "recalling_firm": "The Coca-Cola Company",
      "address_1": "Po Drawer 1734",
      "address_2": "N/A",
      "postal_code": "30301",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "CA",
      "recall_number": "F-0561-2017",
      "product_description": "Dr. Pepper Cherry, 12oz (12 pack cans), Manufactured under the authority of Doctor Pepper  Company, 5301 Legacy Drive, Plano, TX.",
      "product_quantity": "1,020 cases",
      "reason_for_recall": "The product contains undeclared High-fructose Corn Syrup (HFCS).",
      "recall_initiation_date": "20160331",
      "center_classification_date": "20161205",
      "termination_date": "20161205",
      "report_date": "20161214",
      "code_info": "Date Code: NOV2116DDB"
    }
  ]
}