{
  "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": "2026-08-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "113605",
      "product_res_number": "Z-0250-2013",
      "event_date_initiated": "2011-11-03",
      "event_date_posted": "2012-11-06",
      "recall_status": "Terminated",
      "event_date_terminated": "2012-11-06",
      "res_event_number": "63369",
      "product_code": "JQP",
      "product_description": "Sunquest Laboratory, version 7.0\n\nnot available",
      "code_info": "not available",
      "firm_fei_number": "1000306472",
      "recalling_firm": "Sunquest Information Systems, Inc.",
      "address_1": "250 S Williams Blvd",
      "city": "Tucson",
      "state": "AZ",
      "postal_code": "85711-4472",
      "additional_info_contact": "520-570-2252",
      "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.",
      "root_cause_description": "Software design",
      "action": "Sunquest Information Systems, Inc. sent a recall letter dated November 3, 2011, to all affected customers.  Customers were informed of the problem identified and the actions to be taken.  Customers were informed that a change request CR11-00174907 has been created to address this issue.  This will be available as part of Sunquest Laboratory version 7.0.1.  To request the software correction, customers were instructed to create a Case via the Client Support webpage at www.sunquestinfo.com/supportweb.  Then choose a new case, and finally select work queue and select software request.  Customers with questions were instructed to call (877) 239-6337 for US and Canadian sites and at +44 (0) 161 335 0562 for international sites.\nFor questions regarding this recall call 520-570-2252.",
      "product_quantity": "14 sites",
      "distribution_pattern": "Worldwide Distribution - USA (nationwide) and Internationally to Ireland",
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