{
  "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": "2026-07-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
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  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Dover Plains",
      "state": "NY",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "96001",
      "recalling_firm": "GNMart LLC",
      "address_1": "7 Sawmill Ln",
      "address_2": "",
      "postal_code": "12522-6086",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Press Release",
      "distribution_pattern": "Nationwide within the United States",
      "recall_number": "D-0170-2025",
      "product_description": "FORCE FOREVER 400mg Tablets, Huesos y articulaciones sin dolor, SUPLEMENTO ALIMENTICIO, 60-count bottles",
      "product_quantity": "374 bottles",
      "reason_for_recall": "Marketed without an approved NDA/ANDA. FDA analysis found the product to be tainted with Diclofenac and Dexamethasone.",
      "recall_initiation_date": "20241212",
      "center_classification_date": "20250102",
      "report_date": "20250108",
      "code_info": "All lots, Exp. Date: 03/27/2030",
      "more_code_info": ""
    }
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}