{
  "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": "2026-09-08",
    "results": {
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          "brand_name": "CYBERKNIFE ROBOTIC RADIOSURGERY SYSTEM",
          "generic_name": "CYBERKNIFE SYSTEM",
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          "openfda": {
            "device_name": "Accelerator, Linear, Medical",
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      "product_problems": [
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      "reporter_state_code": "WI",
      "manufacturer_zip_code": "",
      "suppl_dates_mfr_received": "",
      "mfr_report_type": "Thirty-Day",
      "manufacturer_contact_country": "",
      "date_changed": "20250813",
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      "summary_report_flag": "N",
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          "sequence_number_treatment": [
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        }
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      "manufacturer_contact_city": "",
      "mdr_report_key": "4071646",
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      "number_devices_in_event": "",
      "date_manufacturer_received": "20140725",
      "manufacturer_name": "",
      "report_source_code": "Manufacturer report",
      "remedial_action": [
        ""
      ],
      "manufacturer_g1_zip_code": "",
      "report_to_manufacturer": "",
      "manufacturer_zip_code_ext": "",
      "manufacturer_g1_name": "",
      "adverse_event_flag": "Y",
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      "single_use_flag": "",
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      "mdr_text": [
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          "mdr_text_key": "12428452",
          "text_type_code": "Additional Manufacturer Narrative",
          "patient_sequence_number": "1",
          "text": "INVESTIGATION HAS DETERMINED THAT THE FIELD ENGINEER NEGLECTED TO DISCHARGE THE CAPACITOR AFTER RE-POWERING ON THE SYSTEM. IN ADDITION, IT WAS REPORTED THAT THERE IS NO SERVICE DOCUMENTATION FOR THIS PROCEDURE. A CAPA HAS BEEN OPENED TO ADDRESS THIS ISSUE. THERE IS NO REPORT OF SYSTEM MALFUNCTION ASSOCIATED WITH THIS EVENT. (B)(4)."
        },
        {
          "mdr_text_key": "4900207",
          "text_type_code": "Description of Event or Problem",
          "patient_sequence_number": "1",
          "text": "IT WAS REPORTED BY AN ACCURACY EMPLOYEE, THAT A FIELD SERVICE ENGINEER RECEIVED AN ELECTRICAL SHOCK WHILE SERVICING THE SYSTEM MODULATOR CABINET AT THE POINT OF THE CIRCUIT BREAKER THREE. THE FIELD SERVICE ENGINEER REPORTED BURNS ON HIS FINGERS AT THE POINT OF ENTRY, ALONG WITH HEART PALPITATIONS AND AN \"UNUSUAL REACTION OF THE NERVOUS SYSTEM.\" THERE IS NO REPORT OF SERIOUS INJURY OR DEATH."
        }
      ],
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      "manufacturer_g1_address_1": "",
      "distributor_zip_code": "",
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      "manufacturer_contact_exchange": "",
      "manufacturer_contact_pcountry": "",
      "suppl_dates_fda_received": ""
    }
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}