{
  "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": "2026-08-27",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "26925",
      "product_res_number": "Z-0807-03",
      "event_date_initiated": "2003-04-01",
      "event_date_posted": "2003-05-09",
      "recall_status": "Terminated",
      "event_date_terminated": "2004-04-21",
      "res_event_number": "26045",
      "product_description": "Misys Laboratory System version 5.3",
      "code_info": "Version 5.3 only.",
      "firm_fei_number": "1000306472",
      "recalling_firm": "Misys Healthcare Systems",
      "address_1": "4801 E Broadway Blvd",
      "city": "Tucson",
      "state": "AZ",
      "postal_code": "85711",
      "additional_info_contact": "Barbara Browne\n520-570-2000",
      "reason_for_recall": "Software anomally, One client reported patient tests and results are deleted when duplicate orders are placed.",
      "root_cause_description": "Other",
      "action": "Notice was sent by fax on 4/1/2003 under Product Safety Notice, PSN-03-L17. A code modification is yet to be released. Customers have been provided with a temporary workaround procedure.",
      "product_quantity": "3",
      "distribution_pattern": "States of MI, OH, NY.",
      "openfda": {}
    }
  ]
}