{
  "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": "Charlotte",
      "state": "NC",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Food",
      "event_id": "76271",
      "recalling_firm": "Coca-Cola Consolidated",
      "address_1": "4901 Chesapeake Dr",
      "address_2": "N/A",
      "postal_code": "28216-2905",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "NC",
      "recall_number": "F-1344-2017",
      "product_description": "Dr. Pepper, 2 Liters (2.1 qt) plastic bottles, Bottled under the authority of Dr. Pepper Company, 5301 Legacy Drive, Plano, TX 75024.",
      "product_quantity": "297 cases (8 bottles/case)",
      "reason_for_recall": "Product labeled Dr. Pepper may instead contain Diet Dr. Pepper (containing undeclared Aspartame as a sweetener).",
      "recall_initiation_date": "20170105",
      "center_classification_date": "20170125",
      "termination_date": "20170130",
      "report_date": "20170201",
      "code_info": "Date Code MAR2717syf"
    }
  ]
}