{
  "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": "63369",
      "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 - USA (nationwide) and Internationally to Ireland",
      "recall_number": "Z-0250-2013",
      "product_description": "Sunquest Laboratory, version 7.0    not available",
      "product_quantity": "14 sites",
      "reason_for_recall": "Sunquest is recalling Sunquest Laboratory version 7.0 because when saving an Accession to a non-current Episode/Event, a User-Defined field can be incorrectly replaced by the current Episode/Event User-Defined data.",
      "recall_initiation_date": "20111103",
      "center_classification_date": "20121106",
      "termination_date": "20121106",
      "report_date": "20121114",
      "code_info": "not available"
    }
  ]
}