{
  "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": [
    {
      "status": "Ongoing",
      "city": "Waukesha",
      "state": "WI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89027",
      "recalling_firm": "GE Healthcare, LLC",
      "address_1": "3000 N Grandview Blvd",
      "address_2": "",
      "postal_code": "53188-1615",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide and US Nationwide Distribution",
      "recall_number": "Z-0242-2022",
      "product_description": "Computed Tomography Systems  Revolution CT,   Revolution CT ES,   Revolution Apex,   Revolution CT with Apex edition",
      "product_quantity": "105 in total",
      "reason_for_recall": "The accumulated dose is incorrectly displayed in certain situations. Thisoccurs during an interventional exam using the SmartStep option if the table height is adjusted after  the exam starts. In this situation, the SmartStep display will show a value that is higher (up to 100  times) than the actual dose delivered.",
      "recall_initiation_date": "20210630",
      "center_classification_date": "20211124",
      "report_date": "20211201",
      "code_info": "Revolution CT,   Revolution CT ES,   Revolution Apex,   Revolution CT with Apex edition",
      "more_code_info": ""
    }
  ]
}