{
  "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": [
    {
      "country": "United States",
      "city": "Santa Clarita",
      "address_1": "21446 Golden Triangle Rd",
      "reason_for_recall": "Marketed without an Approved NDA/ANDA: Products contain undeclared active pharmaceutical ingredients; desmethyl carbondenafil and dapoxetine.",
      "address_2": "",
      "product_quantity": "337 bottles",
      "code_info": "All lots",
      "center_classification_date": "20160216",
      "distribution_pattern": "Nationwide",
      "state": "CA",
      "product_description": "Rhino 7 3000, 6 count Bottle, Distributed by Rhino 7, Made in USA",
      "report_date": "20160224",
      "classification": "Class I",
      "openfda": {},
      "recalling_firm": "Premiere Sales Group",
      "recall_number": "D-0672-2016",
      "initial_firm_notification": "E-Mail",
      "product_type": "Drugs",
      "event_id": "72522",
      "termination_date": "20170601",
      "more_code_info": "",
      "recall_initiation_date": "20150930",
      "postal_code": "91350-2911",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}