{
  "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": "Cleveland",
      "state": "OH",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "76144",
      "recalling_firm": "Philips Medical Systems (Cleveland) Inc",
      "address_1": "595 Miner Rd",
      "address_2": "N/A",
      "postal_code": "44143-2131",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Product was not distributed in the US.    Unit was distributed in Australia.",
      "recall_number": "Z-1058-2017",
      "product_description": "Brilliance iCT",
      "product_quantity": "1-unit",
      "reason_for_recall": "During a retrospective review of production documentation it was observed that the M6 Rotor Counterweight Bolt may have been improperly torqued.",
      "recall_initiation_date": "20161223",
      "center_classification_date": "20170120",
      "termination_date": "20180626",
      "report_date": "20170201",
      "code_info": "Rotor-4535-673-94382 SN 19,  installed on Brilliance ICT System S/N 200203"
    }
  ]
}