{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Austin",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "86358",
      "recalling_firm": "Luminex Corporation",
      "address_1": "12212 Technology Blvd",
      "address_2": "N/A",
      "postal_code": "78727-6101",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Other",
      "distribution_pattern": "US distribution in MO.    No OUS",
      "recall_number": "Z-0054-2021",
      "product_description": "VERIGENE Processor SP  Model No. 10-0000-07.  An in vitro diagnostic device intended for processing and identifying nucleic acids",
      "product_quantity": "1 system",
      "reason_for_recall": "No results/incorrect results due to failure of the hybridization heater.",
      "recall_initiation_date": "20181210",
      "center_classification_date": "20201005",
      "report_date": "20201014",
      "code_info": "Catalogue Number:  10-0000-07  Serial No. 14230205  UDI Code: 00857573006010"
    }
  ]
}