{
  "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": "Overland Park",
      "state": "KS",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "79842",
      "recalling_firm": "Epic Products, LLC",
      "address_1": "11730 W 135th St",
      "address_2": "#224",
      "postal_code": "66221-9395",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Press Release",
      "distribution_pattern": "Nationwide in the USA",
      "recall_number": "D-0288-2019",
      "product_description": "Euphoric Premium Male Performance Enhancer capsules, packaged in a)1-count blister cards, UPC 6 96859 28646 9, b) 3-count bottle, UPC 6 96859 28647 6 and c) 12-count bottle, UPC 6 96859 28648 3.",
      "product_quantity": "a) 106,329 cards; b) 109,725 bottles; c) 28,644 bottles",
      "reason_for_recall": "Marketed Without An Approved NDA/ANDA: product contains undeclared sildenafil, tadalafil, and oxytetracycline, FDA approved drug products making Euphoric an unapproved drug.",
      "recall_initiation_date": "20180416",
      "center_classification_date": "20181130",
      "termination_date": "20241003",
      "report_date": "20181121",
      "code_info": "All lots",
      "more_code_info": ""
    }
  ]
}