{
  "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": "31796",
      "product_res_number": "Z-0727-04",
      "event_date_initiated": "2004-02-27",
      "event_date_posted": "2004-07-20",
      "recall_status": "Terminated",
      "event_date_terminated": "2005-11-17",
      "res_event_number": "28410",
      "product_code": "MSX",
      "k_numbers": [
        "K020524"
      ],
      "product_description": "PatientNet Monitoring System -  PatientNet Central Stations utilizing software Versions 1.03.14, 1.04xx, 2.00xx.",
      "code_info": "All PatientNet Central Stations",
      "firm_fei_number": "2124823",
      "recalling_firm": "General Electric Medical Systems Information Technology",
      "address_1": "8200 W Tower Ave",
      "city": "Milwaukee",
      "state": "WI",
      "postal_code": "53223-3219",
      "reason_for_recall": "Non-invasive blood pressure readings on central station may not match bedside monitor due to software anomaly.",
      "root_cause_description": "Other",
      "action": "Consignees were notified via certified mail, return receipt requested, on Friday, February 27, 2004.  GE Field service representatives will upgrade affected PatientNet Central Stations (RVS, IRVS, or Sitelink IRVS) to software version 2.01.",
      "product_quantity": "Undetermined a this time. 574 sofware units were distributed with ability to upgrade one or multiple devices.",
      "distribution_pattern": "Nationwide throughout the United States",
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}