{
  "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",
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      "manufacturer_address_2": "",
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      "date_of_event": "20111017",
      "reprocessed_and_reused_flag": "N",
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      "exemption_number": "",
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      "manufacturer_contact_area_code": "",
      "date_added": "20111117",
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          "brand_name": "DA VINCI SURGICAL SYSTEM",
          "generic_name": "ENDOSCOPIC INSTRUMENT CONTROL SYSTEM",
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          "manufacturer_d_address_2": "",
          "manufacturer_d_city": "SUNNYVALE",
          "manufacturer_d_state": "CA",
          "manufacturer_d_zip_code": "",
          "manufacturer_d_zip_code_ext": "",
          "manufacturer_d_country": "",
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          "device_operator": "HEALTH PROFESSIONAL",
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          "lot_number": "",
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          "device_evaluated_by_manufacturer": "R",
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            "medical_specialty_description": "Gastroenterology, Urology",
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      "reporter_state_code": "NJ",
      "manufacturer_zip_code": "",
      "suppl_dates_mfr_received": "",
      "mfr_report_type": "Thirty-Day",
      "manufacturer_contact_country": "",
      "date_changed": "20250806",
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      "manufacturer_contact_extension": "",
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          "date_received": "20111116",
          "sequence_number_treatment": [
            "DA VINCI SURGICAL SYS INSTRUMENTS AND ACCESSORIES"
          ],
          "sequence_number_outcome": [
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          ],
          "patient_age": "32 YR",
          "patient_sex": "",
          "patient_weight": "",
          "patient_ethnicity": "",
          "patient_race": "",
          "patient_problems": [
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            "Tissue Damage"
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        }
      ],
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      "date_report": "20111017",
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      "manufacturer_g1_country": "",
      "manufacturer_contact_city": "",
      "mdr_report_key": "2339742",
      "removal_correction_number": "",
      "number_devices_in_event": "",
      "date_manufacturer_received": "20111017",
      "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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      "manufacturer_state": "",
      "distributor_address_2": "",
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      "single_use_flag": "",
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      "mdr_text": [
        {
          "mdr_text_key": "2352487",
          "text_type_code": "Description of Event or Problem",
          "patient_sequence_number": "1",
          "text": "IT WAS REPORTED THAT DURING A DA VINCI HYSTERECTOMY PROCEDURE THE SURGEON ACCIDENTALLY CUT THE PATIENT'S HYPOGASTRIC NERVE. THE PROCEDURE WAS CONVERTED TO TRADITIONAL OPEN SURGICAL TECHNIQUES TO COMPLETE THE PLANNED PROCEDURE AND REPAIR THE PATIENT'S HYPOGASTRIC NERVE. NO SYSTEM MALFUNCTION OCCURRED."
        },
        {
          "mdr_text_key": "9487599",
          "text_type_code": "Additional Manufacturer Narrative",
          "patient_sequence_number": "1",
          "text": "BASED ON THE INFORMATION PROVIDED BY HOSPITAL, IT WAS DETERMINED THAT THE DA VINCI SURGICAL SYSTEM WORKED AS INTENDED, NO SYSTEM MALFUNCTION OCCURRED AND THE SYSTEM DID NOT CAUSE OR CONTRIBUTE TO THE PATIENT'S INJURY."
        }
      ],
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      "distributor_zip_code": "",
      "manufacturer_contact_postal_code": "",
      "manufacturer_contact_exchange": "",
      "manufacturer_contact_pcountry": "",
      "suppl_dates_fda_received": ""
    }
  ]
}