{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "country": "United States",
      "city": "Waukesha",
      "address_1": "3000 N Grandview Blvd",
      "reason_for_recall": "Intermittently not receiving an audible exposure indication upon completion of an exposure on the Proteus stationary radiographic system.",
      "address_2": "",
      "product_quantity": "647 US; 167 OUS",
      "code_info": "console part number 5441870) and (console spare  part numbers 5462233, 5462233-R, 5761170, 5462233-H)",
      "center_classification_date": "20190920",
      "distribution_pattern": "Worldwide - US Nationwide",
      "state": "WI",
      "product_description": "Proteus XR/a (SlOK : K993090)",
      "report_date": "20191002",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "GE Healthcare, LLC",
      "recall_number": "Z-2449-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "83647",
      "more_code_info": "",
      "recall_initiation_date": "20190809",
      "postal_code": "53188-1615",
      "voluntary_mandated": "FDA Mandated",
      "status": "Ongoing"
    }
  ]
}