{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Northbrook",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92451",
      "recalling_firm": "Luminex Corporation",
      "address_1": "4088 Commercial Ave",
      "address_2": "N/A",
      "postal_code": "60062-1829",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Worldwide and US Nationwide Distribution",
      "recall_number": "Z-2024-2023",
      "product_description": "VERIGENE Clostridium difficile Nucleic Acid Test, REF 30-002-022",
      "product_quantity": "114 units",
      "reason_for_recall": "It is possible that in rare instances the VERIGENE CDF Nucleic Acid Test Kit (Part No. 20-005-022) and the VERIGENE Enteric Pathogens Nucleic Acid Test Kit (Part No. 20-005-023) could provide a false-negative result due to hydrophobic characteristics in specific FLOQSwab lots.",
      "recall_initiation_date": "20230605",
      "center_classification_date": "20230628",
      "report_date": "20230705",
      "code_info": "UDI/DI , Lot Numbers:  071222022D, 100622022D",
      "more_code_info": ""
    }
  ]
}