{
  "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": {
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      "status": "Ongoing",
      "city": "West Sacramento",
      "state": "CA",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "92203",
      "recalling_firm": "Gadget Island, Inc",
      "address_1": "1275 Halyard Dr Ste 175",
      "address_2": "",
      "postal_code": "95691",
      "voluntary_mandated": "Voluntary: Firm initiated",
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      "distribution_pattern": "Nationwide in the USA.",
      "recall_number": "D-0573-2023",
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      "product_quantity": "140 blister packs",
      "reason_for_recall": "Marketed without an Approved NDA/ANDA: FDA analysis found product to be tainted with 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": "20230426",
      "center_classification_date": "20230511",
      "report_date": "20230510",
      "code_info": "Lot/Item#: OMS760-B, Exp: 12/2025",
      "more_code_info": ""
    }
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}