{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Waukesha",
      "address_1": "3000 N Grandview Blvd",
      "reason_for_recall": "GE Healthcare has recently become aware of a potential safety issue that may result in the loss of C-arm gantry motion capability on fluoroscopic Interventional imaging systems (Innova, Optima and Discovery).",
      "address_2": "",
      "product_quantity": "10",
      "code_info": "Serial Number                System ID  0000013C2S0065 302421IGS520  15C2R0058 LVIGS2  15C2R0065 AM1396F508  15C2R0082 206598UIGS  15C2R0092 AM135FE37  0000015C2R0062 HU1117VA01  0000015C2R0057 083016848125215  0000015C2R0069 5512XR0026   0000015C2R0060 00632VAS01  0000015C2R0080 00391VAS02",
      "center_classification_date": "20150702",
      "distribution_pattern": "Worldwide Distribution: US (nationwide) including states of: CA, DE, FL, GA, IL, IN, KS, MS, NV, OH, OK, OR, PA, TN, TX, VA, WA and WI; and countries of: ARGENTINA, BELGIUM, BRAZIL, CANADA, CHILE, CHINA, FRANCE, GERMANY, HONG KONG, HUNGARY, INDIA, INDONESIA, ITALY, JAPAN, RUSSIA, UNITED KINGDOM, and VIETNAM.",
      "state": "WI",
      "product_description": "GE Healthcare Innova IGS 520.    Angiographic X-ray systems used in generating fluoroscopic and rotational images of human anatomy for diagnostic, interventional and image-guided surgical procedures.",
      "report_date": "20150708",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "GE Healthcare",
      "recall_number": "Z-1980-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "71508",
      "termination_date": "20151028",
      "more_code_info": "",
      "recall_initiation_date": "20150529",
      "postal_code": "53188-1615",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}