{
  "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": "2026-04-08",
    "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": "88116",
      "recalling_firm": "GE Healthcare, LLC",
      "address_1": "3000 N Grandview Blvd",
      "address_2": "N/A",
      "postal_code": "53188-1615",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "3,665 (US = 956; OUS = 2,709)",
      "recall_number": "Z-1900-2021",
      "product_description": "Revolution EVO, Optima CT660, Optima CT680 CT Systems.",
      "product_quantity": "3665",
      "reason_for_recall": "Improperly loaded software options may result in additional X -ray radiation exposure to the patient.",
      "recall_initiation_date": "20210614",
      "center_classification_date": "20210625",
      "report_date": "20210707",
      "code_info": "Optima CT660  12HW28.8  14HW30.3  15HW25.2  13HW38.14  15HW13.7  Revolution EVO  14HW17.4  15HW13.7  Optima CT680  13HW38.14  15BW21.2"
    }
  ]
}