{
  "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,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Jamestown",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "97117",
      "recalling_firm": "Trinity Biotech USA",
      "address_1": "2823 Girts Rd",
      "address_2": "N/A",
      "postal_code": "14701-9666",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide - US Nationwide distribution in the states of Maryland and Utah.  The countries of France, Germany, Ireland, Israel, Kuwait, Latvia, UK.",
      "recall_number": "Z-2292-2025",
      "product_description": "Bartels ELISA Legionella Urinary Antigen. Model Number: B1029-440.    In Vitro Diagnostic test kit for the presumptive diagnosis of past or current Legionnaires  Disease.",
      "product_quantity": "968 kits",
      "reason_for_recall": "Potential for Bartels ELISA Legionella Urinary Antigen kit B1029-440 lot 065 and 066 to contain particulate matter.",
      "recall_initiation_date": "20250722",
      "center_classification_date": "20250812",
      "report_date": "20250820",
      "code_info": "Model Number: B1029-440. UDI-DI: 05391516744065. Lot Numbers: 065 and 066",
      "more_code_info": ""
    }
  ]
}