{
  "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": "63380",
      "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": "Nationwide Distribution.",
      "recall_number": "Z-0251-2013",
      "product_description": "Sunquest Application Interfacing Outbound Phlebotomy Point of Care Interface, v3.0.0_07222004 and later.",
      "product_quantity": "9 units",
      "reason_for_recall": "The recall was initiated because Sunquest Information System has confirmed reports of an Outbound Phlebotomy Point of Care (POC) interface is combining patient orders inappropriately.",
      "recall_initiation_date": "20091119",
      "center_classification_date": "20121106",
      "termination_date": "20121106",
      "report_date": "20121114",
      "code_info": "v3.0.0_07222004 and later"
    }
  ]
}