{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Waukesha",
      "state": "WI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "66168",
      "recalling_firm": "GE Healthcare, LLC",
      "address_1": "3000 N Grandview Blvd",
      "address_2": "N/A",
      "postal_code": "53188-1615",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution: US (nationwide) including states of : PA and TN; countries of: FRANCE and SINGAPORE.",
      "recall_number": "Z-2253-2013",
      "product_description": "GE Healthcare Discovery IGS 730 Cardiovascular X-Ray Imaging System.    The angiography X-ray systems are indicated for use in generating fluoroscopic and rotational images of human anatomy for cardiovascular, vascular and non-vascular, diagnostic and interventional procedures. Additionally, with the OR table, the angiographic X-ray systems are indicated for use in generating fluoroscopic and rotational images of human anatomy for image guided surgical procedures. The OR table is suitable for interventional and surgical procedures.",
      "product_quantity": "4 (2 US, 2 OUS)",
      "reason_for_recall": "GE Healthcare has recently become aware of a potential safety issue with respect to Discovery IGS 730 Imaging Systems.    A patient data management error may prevent the Discovery IGS 730 Imaging System from booting on start-up or re-booting during procedure. The boot issue may occur when a large  amount of patient data remains in the browser and is not deleted. The inability to boot the system ma",
      "recall_initiation_date": "20130619",
      "center_classification_date": "20130918",
      "termination_date": "20131025",
      "report_date": "20130925",
      "code_info": "Mfg Lot or Serial #  00000611882BU2  00000612803BU7  00000613979BU4  00000620447BU3",
      "more_code_info": ""
    }
  ]
}