{
  "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": [
    {
      "status": "Terminated",
      "city": "Tucson",
      "state": "AZ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "62714",
      "recalling_firm": "Sunquest Information Systems, Inc.",
      "address_1": "250 S Williams Blvd",
      "address_2": "N/A",
      "postal_code": "85711-4472",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution, including Nationwide (USA) and the countries of Canada, Denmark, Ireland, the United Arab Emirates and the United Kingdom.",
      "recall_number": "Z-2272-2012",
      "product_description": "Sunquest Laboratory LabAccess Results Workstation (LARS)",
      "product_quantity": "151 sites",
      "reason_for_recall": "The recall was initiated because Sunquest has confirmed that the Sunquest Laboratory LabAccess Results Workstation (LARS) may file results to the wrong patient by incorrectly combining results.",
      "recall_initiation_date": "20101005",
      "center_classification_date": "20120824",
      "termination_date": "20120824",
      "report_date": "20120905",
      "code_info": "Sunquest Laboratory versions 5.3.3 and 6.3.0 SP3"
    }
  ]
}