{
  "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": "2026-07-29",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Brentwood",
      "state": "NY",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "89563",
      "recalling_firm": "Celebrate Today",
      "address_1": "143 Front Ave",
      "address_2": "N/A",
      "postal_code": "11717-5113",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Press Release",
      "distribution_pattern": "Product was distributed nationwide in the USA via Amazon Marketplace",
      "recall_number": "D-0638-2022",
      "product_description": "RED MAMMOTH capsules, 400 mg, packaged in 10-count blisters per carton, ASIN B00KA8FBNI, barcode X001ANE0I5.",
      "product_quantity": "500 cartons",
      "reason_for_recall": "Marketed Without An Approved NDA/ANDA: Product was found to contain undeclared sildenafil and tadalafil, ingredients found in FDA approved products for the treatment of male sexual enhancement, making this an unapproved drug.",
      "recall_initiation_date": "20220208",
      "center_classification_date": "20220228",
      "termination_date": "20220329",
      "report_date": "20220223",
      "code_info": "Lot # DK1027, Exp. 08/01/2023"
    }
  ]
}