{
  "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": "Greenville",
      "state": "SC",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Food",
      "event_id": "75738",
      "recalling_firm": "Nutra Manufacturing",
      "address_1": "1050 Woodruff Rd",
      "address_2": "N/A",
      "postal_code": "29607-4120",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "PA",
      "recall_number": "F-0626-2017",
      "product_description": "GNC, Women\u0019s Ultra Mega, Dietary Supplement, 180 Caplets,",
      "product_quantity": "12,534 bottles/180 caplets per bottle.",
      "reason_for_recall": "Undeclared Allergen: Milk.",
      "recall_initiation_date": "20161110",
      "center_classification_date": "20161207",
      "termination_date": "20170727",
      "report_date": "20161214",
      "code_info": "GNC number: 202422, Nutra Manufacturing Lot Number: 3044FQ2024."
    }
  ]
}