{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Andover",
      "address_1": "3000 Minuteman Rd",
      "reason_for_recall": "The MX40 may experience increased power consumption and may have a lack of visual and/or audible notifications while in a  Low Battery State .",
      "address_2": "",
      "product_quantity": "",
      "code_info": "All revision B.X versions are affected.",
      "center_classification_date": "20190531",
      "distribution_pattern": "Worldwide distribution - US Nationwide and to 71 countries.",
      "state": "MA",
      "product_description": "IntelliVue MX40 Patient Monitor, Product number 865351, Service Numbers  All other countries: 453564451791, 453564451811, 453564467721, 453564467741, 453564467761, 453564467781, 453564467801, 453564467821, 453564467841, 453564467861, 453564262531, and 453564262551 - Product Usage: Used primarily as a traditional telemetry medical device. It connects to the IntelliVue Information Center by way of a wireless network. When the MX40 is connected to the IntelliVue Information Center the IntelliVue Information Center provides the primary patient monitoring and alarming function. The MX40 does not automatically provide local monitoring or alarming when connected to the Information Center.",
      "report_date": "20190612",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Philips North  America, LLC",
      "recall_number": "Z-1693-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "82696",
      "more_code_info": "",
      "recall_initiation_date": "20190328",
      "postal_code": "01810-1032",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Ongoing"
    }
  ]
}