{
  "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": [
    {
      "country": "United States",
      "city": "Cleveland",
      "address_1": "595 Miner Rd",
      "reason_for_recall": "Failure to correctly document the installation of four M12 Bolts into the system rotor.",
      "address_2": "",
      "product_quantity": "1",
      "code_info": "Model Number 728306; System Serial Number 100619  Rorot-45535-673-94382 SN26",
      "center_classification_date": "20170111",
      "distribution_pattern": "The one system was distributed in Canada.      There were no government or US distribution.",
      "state": "OH",
      "product_description": "Brilliance iCT    Product  Usage:  Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These devices may include signal analysts and display equipment, patient and equipment supports, components, and accessories",
      "report_date": "20170118",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Philips Medical Systems (Cleveland) Inc",
      "recall_number": "Z-1004-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "76021",
      "termination_date": "20180702",
      "more_code_info": "",
      "recall_initiation_date": "20161125",
      "postal_code": "44143-2131",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}