{
  "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": "17",
      "code_info": "Serial Number                System ID  Not Available 702731CATH3  0000013C2R0003 6012883100CV4  15C2R0084 702880CATH2  15C2R0086 GON4300165  15C2R0085 918787530  15C2R0087 814877EP  0000015C2R0091 GON1441141  0000014C2R0188 XV650620BU8  0000015C2R0083 GON1487269  0000015C2R0088 GON4271086  0000015C2R0064 080041RX18  15C2R0055 414649IGS2  15C2R0072 GON4211904  0000015C2R0074 0004077351  0000015C2R0066 082416190029  0000015C2R0070 082416100092  0000015C2R0071 082416190026",
      "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 530.    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-1981-2015",
      "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"
    }
  ]
}