{
  "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": "2026-08-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "131689",
      "product_res_number": "Z-0426-2015",
      "event_date_initiated": "2014-11-10",
      "event_date_posted": "2014-12-17",
      "recall_status": "Terminated",
      "event_date_terminated": "2015-06-29",
      "res_event_number": "69846",
      "product_code": "RCE",
      "product_description": "GE Cabinet X-ray systems",
      "code_info": "XXL cabinet x-ray systems, serial numbers A586590 and A586780; xlcube compact cabinet x-ray systems, serial numbers A583730, A586430, and A586460; a VTOMEX C450 cabinet x-ray system, serial number VTXO1JOOO2-2245 14; VTOMEX L300 cabinet x-ray systems, serial numbers VTX01lF007-208813, VTX01F007-196312 and VTXO1FOO07-1946 12; and VTOMEX L450 cabinet x-ray systems, serial numbers VTXO1K0001-184711 and PX_10E000-179013.",
      "firm_fei_number": "2519904",
      "recalling_firm": "GE Inspection Technologies, LP",
      "address_1": "50 Industrial Park Rd",
      "city": "Lewistown",
      "state": "PA",
      "postal_code": "17044-9312",
      "additional_info_contact": "Customer Support\n717-447-1278",
      "reason_for_recall": "GE discovered these cabinet x-ray systems' potential failure to comply with the Cabinet X-ray System performance standards.",
      "root_cause_description": "Radiation Control for Health and Safety Act",
      "action": "GE intends to notify its customers of the affected cabinet x-ray systems regarding the warning signs' potential failure to comply with 21 C.F.R.  1020.40(c)(7)(v) through a Technical Information Letter. The notification will inform customers that GE plans to replace the current warning signs with warning signs that comply with the requirements set forth in 21 C.F.R.  1020.40(c)(7)(v). \r\n\r\nGE will recommend in its notification that it replace the warning sign at the customer's next service interval, but no later than December 31, 2014.\r\n\r\nFor further questions please call (717) 447-1278.",
      "product_quantity": "11",
      "distribution_pattern": "US Distribution to the states of MI, PA, NH, CA, OR, WA, NC, IN and SC.",
      "openfda": {
        "device_name": "Cabinet X-Ray, Industrial",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "N"
      }
    }
  ]
}