{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Austin",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89303",
      "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": "E-Mail",
      "distribution_pattern": "Worldwide distribution - US Nationwide distribution in the states of Alabama, California, Georgia, Kansas, Kentucky, Louisiana, Massachusetts, Michigan, Minnesota, Missouri, Nebraska, New Jersey, New Mexico, Ohio, Oklahoma, Oregon, Pennsylvania, Tennessee, Texas, Vermont, Virginia, Washington, Wisconsin and the country of Taiwan.",
      "recall_number": "Z-0498-2022",
      "product_description": "ARIES HSV 1&2 Assay, Part Number/REF 50-10017",
      "product_quantity": "296 kits",
      "reason_for_recall": "Impacted lot may leak inside the ARIES instrument.",
      "recall_initiation_date": "20210416",
      "center_classification_date": "20220114",
      "termination_date": "20240920",
      "report_date": "20220126",
      "code_info": "Lot number AB1703A"
    }
  ]
}