{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Austin",
      "address_1": "12212 Technology Blvd",
      "reason_for_recall": "The hand-held barcode scanner that is used as an accessory to enter ARIES cassette and specimen identifications on the ARIES Systems populates patient sample IDs with a previously scanned sample ID when entering orders into an ARIES instrument.",
      "address_2": "",
      "product_quantity": "15 units",
      "code_info": "ARIES System UDI:  00840487101537 and ARIES M1 System UDI:  00840487100080",
      "center_classification_date": "20170516",
      "distribution_pattern": "Worldwide Distribution - US Distribution and to the countries of Finland and China.",
      "state": "TX",
      "product_description": "ARIES System and ARIES M1 System",
      "report_date": "20170524",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Luminex Corporation",
      "recall_number": "Z-2094-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "77052",
      "termination_date": "20171020",
      "more_code_info": "",
      "recall_initiation_date": "20170419",
      "postal_code": "78727-6101",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}