{
  "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": "Owasso",
      "state": "OK",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Food",
      "event_id": "77506",
      "recalling_firm": "GnuPharma Corp.",
      "address_1": "8751 N 117th East Ave Ste J",
      "address_2": "N/A",
      "postal_code": "74055-2098",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "US",
      "recall_number": "F-0300-2017",
      "product_description": "GnuPharma Foundation 100% Herbal Supplement 60 Capsules",
      "product_quantity": "9 bottles",
      "reason_for_recall": "1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)",
      "recall_initiation_date": "20170508",
      "center_classification_date": "20170718",
      "termination_date": "20181115",
      "report_date": "20170726",
      "code_info": "products manufactured prior to May 8th, 2017."
    }
  ]
}