{
  "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
    }
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  "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": "8",
      "code_info": "Serial Number                System ID  0000012CC20012 YV1950  00000641154BU0 YV1915  646036BU4 412647IR1  00000649367BU0 HCAALL630  00000656468BU6 5973XR0014  00000656469BU4 5973XR0013  657273BU9 936539CL5  Not Available 082416040067",
      "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 630.    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-1984-2015",
      "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"
    }
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}