{
  "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,
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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": "13",
      "code_info": "Serial Number                System ID  00000465837BU3 610776INNOVA21  00000007C20214 760940INNOVA2  00000008C20031 083016842102488  00000007C20126 083016242100487  00000459677BU1 00888VAS02  0000011C2M0208 727869EP4  0000009C2M0034 083016608167379  0000009C2M0022 083016202100349  Not Available 0835160049  0000012C2S0028 A5403911  00000464565BU1 M2844529  0000011BC20026 2192632121  FMI12181DUMM17 082416270004  00000466838BU0 082416160007",
      "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 2100IQ.    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-1976-2015",
      "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"
    }
  ]
}