{
  "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": "Andover",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "64507",
      "recalling_firm": "Philips Healthcare Inc.",
      "address_1": "3000 Minuteman Road",
      "address_2": "N/A",
      "postal_code": "01810",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution: US (nationwide) and country of: Canada.",
      "recall_number": "Z-1783-2014",
      "product_description": "Philips IntellVue Info Center iX 866023; PIIC iX Upgrade 866024; IntellVue Server iX Upgrade 866026; PIIC Classic Upgrade 866117  Patient Physiological Monitor.",
      "product_quantity": "899",
      "reason_for_recall": "If a customer creates customized trend scales in the trend review tile and the iX or primary server reboots for any reason, the iX(s) will enter a reboot loop.  If one iX reboots, the issue will impact only those patients monitored on that device.  If the primary server reboots, all patients across all iX devices will be impacted.",
      "recall_initiation_date": "20130305",
      "center_classification_date": "20140611",
      "termination_date": "20170517",
      "report_date": "20140618",
      "code_info": "All iX versions with A.01 software"
    }
  ]
}