{
  "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
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "El Paso",
      "state": "TX",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "93257",
      "recalling_firm": "Botanical Be",
      "address_1": "360 Jardin Bello",
      "address_2": "",
      "postal_code": "79932-2357",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "USA Nationwide",
      "recall_number": "D-0226-2024",
      "product_description": "Kuka Flex Forte caplets, packaged in 30-count bottles, Manufactured by: Kukamonga, Gonzalez Ortega No 170 Col Centro, 44100 Guadalajara Jal, UPC 0736640810265",
      "product_quantity": "300 bottles",
      "reason_for_recall": "Marketed Without an Approved NDA/ANDA: products found to contain undeclared diclofenac.",
      "recall_initiation_date": "20231020",
      "center_classification_date": "20240112",
      "report_date": "20231206",
      "code_info": "All lots, exp 12/12/2024",
      "more_code_info": ""
    }
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}