{
  "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": "Ferndale",
      "state": "MI",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "82594",
      "recalling_firm": "SELECT DISTRIBUTIONS LLC",
      "address_1": "1320 W 9 Mile Rd",
      "address_2": "N/A",
      "postal_code": "48220",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "MI, OH",
      "recall_number": "D-1344-2019",
      "product_description": "Aphrodisiac Platinum 40000, Proprietary Raw Material 6000 mg, 1 count blister card, 24 cards per box, Distributed by:  APhrodisiac. UPC Code 644118128135",
      "product_quantity": "60 boxes",
      "reason_for_recall": "Marketed without an approved NDA/ANDA: FDA analysis has found the product to be tainted with sildenafil",
      "recall_initiation_date": "20190409",
      "center_classification_date": "20190613",
      "termination_date": "20231016",
      "report_date": "20190619",
      "code_info": "All lots"
    }
  ]
}