{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Northbrook",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90129",
      "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": "US",
      "recall_number": "Z-1109-2022",
      "product_description": "VERIGENE Nucleic Acid Test Kit-BC-GN Extraction Tray - 9.73 mL, REF 20-009-021",
      "product_quantity": "984 units",
      "reason_for_recall": "Higher than normal \"No Call Internal Control failures\" due to a missing reagent within a small subset of the extraction tray lot.",
      "recall_initiation_date": "20220215",
      "center_classification_date": "20220517",
      "report_date": "20220525",
      "code_info": "Lot Number 101321021B",
      "more_code_info": ""
    }
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}