{
  "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": "Austin",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90698",
      "recalling_firm": "Luminex Corporation",
      "address_1": "12212 Technology Blvd",
      "address_2": "",
      "postal_code": "78727-6101",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S. Nationwide distribution in the states of NE, TX, MS, TN, KY, ME, CA.",
      "recall_number": "Z-1524-2022",
      "product_description": "ARIES SARS-CoV-2 Assay",
      "product_quantity": "257",
      "reason_for_recall": "SARS-CoV-2 assay that detects SARS-CoV-2 ORF1ab and N genes may not detect the ORF1ab gene. A positive results if either SARS-CoV-2 genes is detected, but If both genes are mistakenly not detected, a false negative result would be generated.",
      "recall_initiation_date": "20220714",
      "center_classification_date": "20220817",
      "report_date": "20220824",
      "code_info": "Lot: AB4042A",
      "more_code_info": ""
    }
  ]
}