{
  "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": "Aston",
      "state": "PA",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "67860",
      "recalling_firm": "Nova Products, Inc.",
      "address_1": "5 Mount Pleasant Rd",
      "address_2": "N/A",
      "postal_code": "19014-1407",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Press Release",
      "distribution_pattern": "Nationwide to retailers and distributors",
      "recall_number": "D-1601-2014",
      "product_description": "Xzone 1200,  750 mg, one capsule per blister pack, Distributed by: Xzone, Orlando, FL 32789",
      "product_quantity": "Unknown",
      "reason_for_recall": "Marketed Without an Approved NDA/ANDA: Nova Products, Inc. of Aston, Pennsylvania is voluntarily recalling XZone 1200because FDA laboratory analysis determined that they contain undeclared amounts of sildenafil and tadalafil, active ingredients of FDA-approved drugs used to  treat erectile dysfunction.",
      "recall_initiation_date": "20140328",
      "center_classification_date": "20140918",
      "termination_date": "20150806",
      "report_date": "20140924",
      "code_info": "Lot# 13071012",
      "more_code_info": ""
    }
  ]
}