{
  "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": "89244",
      "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 New Jersey, California, Connecticut, Minnesota, Missouri, New Jersey, New Mexico, Pennsylvania, Tennessee, Washington, and Wisconsin) and the country of Malaysia.",
      "recall_number": "Z-0553-2022",
      "product_description": "ARIES HSV 1&2 Assay, Catalog/REF# 50-10017",
      "product_quantity": "329",
      "reason_for_recall": "Impacted lot may leak inside the ARIES instrument. Testing confirmed a leak rate of 0.9%. Leaking cassettes could potentially lead to incorrect results or a delay in reporting results due to an Invalid.",
      "recall_initiation_date": "20211117",
      "center_classification_date": "20220202",
      "termination_date": "20240708",
      "report_date": "20220209",
      "code_info": "Lot Numbers AB3600A and AB3560A"
    }
  ]
}