{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Plano",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Food",
      "event_id": "78043",
      "recalling_firm": "ProSupps USA LLC",
      "address_1": "2801 E Plano Pkwy",
      "address_2": "N/A",
      "postal_code": "75074-7418",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US and Canada",
      "recall_number": "F-3600-2017",
      "product_description": "DNPX Powder, 30 Pineapple Punch",
      "product_quantity": "40 units",
      "reason_for_recall": "Product contains the unapproved ingredient, picamilon.",
      "recall_initiation_date": "20170830",
      "center_classification_date": "20170929",
      "termination_date": "20180206",
      "report_date": "20171011",
      "code_info": "RLA134860315, RL105080815, RL134660315",
      "more_code_info": ""
    }
  ]
}