{
  "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": "The DoseRight feature suggest a mAs based on the measured patient size, a reference size and a reference mAs.  When scanning large children, the suggested mAs may be higher than clinicians would expect.",
      "address_2": "",
      "product_quantity": "23",
      "code_info": "Brilliance iCT: Model Number 728311 and 728306, Serial Number: 100103, 100019, 100023, 100170, 200047, 200013 200005 and 100087.  Brilliance 64: Model Number 728231 and 728326, Seial Number: 4003, 9745, 9875, 90135, 90169, 95414, 300003, 300004, 300005 and 300010.  Brilliance CT Big Bore, Model Number: 728243, Serial Number: 7006, 7060, 7154, 7298 and 7349.",
      "center_classification_date": "20140129",
      "distribution_pattern": "Worldwide Distribution - US Distribution including the states of DC, IL, IN, MI, MO, NY, OH, OR, PA, TX and VT., and the countries of  Australia, Belgium, China, Germany, India, Israel, Italy and The Netherlands.",
      "state": "OH",
      "product_description": "Brilliance iCT, Brilliance 64 and Brilliance Big Bore    The Brilliance iCT, Brilliance 64 and Brilliance Big Bore are 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 analysis and display equipment, patient, and equipment supports, components and accessories.",
      "report_date": "20140205",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Philips Medical Systems (Cleveland) Inc",
      "recall_number": "Z-0791-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "66311",
      "termination_date": "20140428",
      "more_code_info": "",
      "recall_initiation_date": "20110307",
      "postal_code": "44143-2131",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}