{
  "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,
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  "results": [
    {
      "status": "Ongoing",
      "city": "National City",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "95520",
      "recalling_firm": "C & A Naturistics",
      "address_1": "2424 Hoover Ave Ste N",
      "address_2": "N/A",
      "postal_code": "91950-8575",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Press Release",
      "distribution_pattern": "Nationwide within the United States",
      "recall_number": "D-0024-2025",
      "product_description": "AK Forte Ortiga y Omega 3 Cont. Neto 100 Tabletas, 400 mg,",
      "product_quantity": "Unknown",
      "reason_for_recall": "Marketed without an Approved NDA/ANDA: FDA analysis found the product to be tainted with undeclared diclofenac and acetaminophen.",
      "recall_initiation_date": "20241008",
      "center_classification_date": "20241022",
      "report_date": "20241030",
      "code_info": "All Lots",
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}