{
  "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": "Las Vegas",
      "state": "NV",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "66839",
      "recalling_firm": "Vitality Research Labs LLC",
      "address_1": "8840 W Russell Rd #245",
      "address_2": "N/A",
      "postal_code": "89148",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Press Release",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-1364-2014",
      "product_description": "vitaliKOR Ready When You Are, Fast Acting Formula Dietary Supplement capsules, 40 count bottle, Distributed by Vitality Research Labs, LLC, Las Vegas, NV 89148.",
      "product_quantity": "11,523 bottles of lot K58Q; 54,255 bottles of lot F50Q",
      "reason_for_recall": "Marketed Without an Approved NDA/ANDA: FDA sampling found undeclared  vardenafil and tadalafil in vitaliKOR capsules",
      "recall_initiation_date": "20131119",
      "center_classification_date": "20140611",
      "termination_date": "20140612",
      "report_date": "20140618",
      "code_info": "LOT K58Q  Exp 01/16  LOT F50Q  Exp 07/16"
    }
  ]
}