{
  "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/",
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      "number_devices_in_event": "",
      "date_manufacturer_received": "20100225",
      "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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      "mdr_text": [
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          "text_type_code": "Description of Event or Problem",
          "patient_sequence_number": "1",
          "text": "IT WAS REPORTED THAT POST A DA VINCI SI THYROIDECTOMY PROCEDURE, THE PATIENT EXPERIENCED NUMBNESS DUE TO RADIAL NERVE DAMAGE."
        },
        {
          "mdr_text_key": "8662735",
          "text_type_code": "Additional Manufacturer Narrative",
          "patient_sequence_number": "1",
          "text": "ON MARCH 18, 2010, THE SURGEON REPORTED THAT THERE WAS NO MALFUNCTION OF THE DA VINCI SI SURGICAL SYSTEM DURING THE PROCEDURE AND THAT THE INJURY TO THE PATIENT'S RADIAL NERVE WAS DUE TO THE PATIENT'S ARM POSITIONING. THE SURGEON WAS UNABLE TO PROVIDE ANY DETAILS CONCERNING THE DATE THAT THE EVENT OCCURRED OR OTHER PATIENT DETAILS, HOWEVER, THE SURGEON STATED THAT THE PATIENT HAS FULLY RECOVERED AND SUSTAINED NO PERMANENT DAMAGE. AS OF MARCH 18, 2010, THERE HAVE BEEN NO REPORTED RECURRENCES OF THE ISSUE AT THIS HOSPITAL."
        }
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      "manufacturer_contact_postal_code": "",
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      "manufacturer_contact_pcountry": "",
      "suppl_dates_fda_received": ""
    }
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}