{
  "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": "Boynton Beach",
      "state": "FL",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "81913",
      "recalling_firm": "Happy Together, Inc.",
      "address_1": "1060 Audace Ave Apt 106",
      "address_2": "N/A",
      "postal_code": "33426-3346",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Press Release",
      "distribution_pattern": "Product was sold over the internet",
      "recall_number": "D-0388-2019",
      "product_description": "5K Premium Enhancement capsule, 5000 mg, 1 count blister card, box of 30, Happy Together Inc., Boynton, FL UPC 649964965644",
      "product_quantity": "N/A",
      "reason_for_recall": "Marketed without an Approved NDA/ANDA; FDA analysis found product to be tainted with undeclared sildenafil and tadalafil",
      "recall_initiation_date": "20190108",
      "center_classification_date": "20190122",
      "termination_date": "20211026",
      "report_date": "20190130",
      "code_info": "All lots within expiry"
    }
  ]
}