{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Opa Locka",
      "state": "FL",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Food",
      "event_id": "85496",
      "recalling_firm": "GOLDEN NUTRITION INC",
      "address_1": "13461 Nw 47th Ave",
      "address_2": "N/A",
      "postal_code": "33054-4317",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Domestic distribution only.",
      "recall_number": "F-0930-2020",
      "product_description": "Biotin 1000mcg, Dietary Supplement, 30 Tablets, Manufactured by: Golden Nutrition",
      "product_quantity": "120 bottles",
      "reason_for_recall": "FDA sample analysis of Biotin 1000mg Lot #1345 showed the product Biotin content to be 0.8% of label claim.",
      "recall_initiation_date": "20200406",
      "center_classification_date": "20200429",
      "termination_date": "20200821",
      "report_date": "20200506",
      "code_info": "Lot #1345     EXP 09/22"
    }
  ]
}