{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Prague 10",
      "state": "",
      "country": "Czech Republic",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98219",
      "recalling_firm": "Immunotech A.S.",
      "address_1": "Radiova 1",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide - US Nationwide distribution in the state of NC and the countries of Germany, Argentina, Netherlands, Hungary, Austria, Belgium, France, Italy.",
      "recall_number": "Z-1369-2026",
      "product_description": "Estrone RIA, REF: DSL8700",
      "product_quantity": "160",
      "reason_for_recall": "The affected Estrone RIA kit lots may rarely give falsely high patient results which might cause Temporary injury of Remote probability. Only in some (very rare) cases may the issue occur.",
      "recall_initiation_date": "20251215",
      "center_classification_date": "20260213",
      "report_date": "20260225",
      "code_info": "UDI: 15099590211615. Lot(Expiration): 251013C(2025-12-30), 251110C(2026-01-27)",
      "more_code_info": ""
    }
  ]
}