{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Lewistown",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "74554",
      "recalling_firm": "GE Inspection Technologies, LP",
      "address_1": "50 Industrial Park Rd",
      "address_2": "N/A",
      "postal_code": "17044-9312",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution to the states of : FL, TN, and TX.",
      "recall_number": "Z-2236-2016",
      "product_description": "GE Inspection Technologies, LP - Phoenix v|tome|x m240 cabinet x-ray systems.    A microfocus CT system used primarily for 3D metrology and analysis.",
      "product_quantity": "4",
      "reason_for_recall": "Radiation emissions which exceeded the limit in the performance standard were detected during maintenance of one system.  The identified cause was insufficient attachment of shielding in the door.  Jostling during delivery was identified as the probable cause of this failure to comply with the performance standard.",
      "recall_initiation_date": "20160302",
      "center_classification_date": "20160722",
      "termination_date": "20170807",
      "report_date": "20160803",
      "code_info": "SN - PA2384"
    }
  ]
}