{
  "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,
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  },
  "results": [
    {
      "status": "Terminated",
      "city": "Doral",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Food",
      "event_id": "77715",
      "recalling_firm": "Duy Drugs Inc.",
      "address_1": "1730 NW 79th Ave",
      "address_2": "N/A",
      "postal_code": "33126-1111",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Domestic distribution only.",
      "recall_number": "F-3355-2017",
      "product_description": "Viva ben Femenine Supplement, Dietary Supplement 30 Softgels",
      "product_quantity": "1800 bottles",
      "reason_for_recall": "Failure to meet with 21 CFR Part 111, CGMPs, assuring identity, purity, and composition of dietary supplements.",
      "recall_initiation_date": "20170721",
      "center_classification_date": "20170808",
      "termination_date": "20190424",
      "report_date": "20170816",
      "code_info": "Lot No. 0117221"
    }
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}