{
  "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_contact_zip_ext": "",
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      "event_location": "",
      "report_to_fda": "",
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      "manufacturer_contact_state": "",
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      "manufacturer_g1_city": "",
      "manufacturer_contact_address_1": "",
      "manufacturer_contact_pcity": "",
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      "report_number": "MW5038369",
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      ],
      "product_problem_flag": "N",
      "date_received": "20140923",
      "manufacturer_address_2": "",
      "pma_pmn_number": "",
      "date_of_event": "20110921",
      "reprocessed_and_reused_flag": "",
      "manufacturer_address_1": "",
      "exemption_number": "",
      "manufacturer_contact_zip_code": "",
      "reporter_occupation_code": "PATIENT",
      "manufacturer_contact_plocal": "",
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      "manufacturer_g1_postal_code": "",
      "manufacturer_g1_state": "",
      "reporter_country_code": "US",
      "manufacturer_contact_area_code": "",
      "date_added": "20141001",
      "manufacturer_contact_f_name": "",
      "previous_use_code": "",
      "device": [
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          "implant_flag": "",
          "date_removed_flag": "",
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          "date_removed_year": "",
          "serviced_by_3rd_party_flag": "",
          "date_received": "20140923",
          "brand_name": "DA VINCI",
          "generic_name": "DA VINCI",
          "manufacturer_d_name": "INTUITIVE SURGICAL INC",
          "manufacturer_d_address_1": "",
          "manufacturer_d_address_2": "",
          "manufacturer_d_city": "",
          "manufacturer_d_state": "",
          "manufacturer_d_zip_code": "",
          "manufacturer_d_zip_code_ext": "",
          "manufacturer_d_country": "",
          "manufacturer_d_postal_code": "",
          "device_operator": "HEALTH PROFESSIONAL",
          "model_number": "",
          "catalog_number": "",
          "lot_number": "",
          "other_id_number": "",
          "device_availability": "",
          "device_report_product_code": "NAY",
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          "device_evaluated_by_manufacturer": "",
          "combination_product_flag": "",
          "udi_di": "",
          "udi_public": "",
          "openfda": {
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            "medical_specialty_description": "Gastroenterology, Urology",
            "regulation_number": "876.1500",
            "device_class": "2"
          }
        }
      ],
      "product_problems": [
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      ],
      "reporter_state_code": "MN",
      "manufacturer_zip_code": "",
      "suppl_dates_mfr_received": "",
      "mfr_report_type": "",
      "manufacturer_contact_country": "",
      "date_changed": "20250825",
      "health_professional": "",
      "summary_report_flag": "N",
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      "manufacturer_contact_extension": "",
      "manufacturer_city": "",
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      "patient": [
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          "date_received": "20140923",
          "sequence_number_treatment": [
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          ],
          "sequence_number_outcome": [
            "Hospitalization",
            " R",
            " S"
          ],
          "patient_age": "54 YR",
          "patient_sex": "",
          "patient_weight": "82",
          "patient_ethnicity": "",
          "patient_race": "",
          "patient_problems": [
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            "Laceration(s)",
            "Therapeutic Response, Decreased"
          ]
        }
      ],
      "distributor_city": "",
      "date_report": "20140923",
      "initial_report_to_fda": "",
      "distributor_state": "",
      "event_key": "",
      "manufacturer_g1_country": "",
      "manufacturer_contact_city": "",
      "mdr_report_key": "4128567",
      "removal_correction_number": "",
      "number_devices_in_event": "",
      "manufacturer_name": "",
      "report_source_code": "Voluntary report",
      "remedial_action": [
        ""
      ],
      "manufacturer_g1_zip_code": "",
      "report_to_manufacturer": "",
      "manufacturer_zip_code_ext": "",
      "manufacturer_g1_name": "",
      "adverse_event_flag": "Y",
      "distributor_address_1": "",
      "manufacturer_state": "",
      "distributor_address_2": "",
      "manufacturer_postal_code": "",
      "single_use_flag": "",
      "manufacturer_country": "",
      "mdr_text": [
        {
          "mdr_text_key": "4943997",
          "text_type_code": "Description of Event or Problem",
          "patient_sequence_number": "1",
          "text": "ON (B)(6) 2011, I HAD A TOTAL HYSTERECTOMY WITH BILATERAL SALPINGO-OOPHORECTOMY USING THE DA VINCI INTERFACE. I SUFFERED A COMPLETE TRANSECTION OF THE RIGHT DISTAL URETER. POST OP I DEVELOPED A FISTULA WITH URETERAL STRICTURE. I HAD A SURGICAL REPAIR ON (B)(6) 2011, WHICH DID NOT CHANGE THE TOTAL URINARY INCONTINENCE I SUFFERED AS A RESULT OF THE INITIAL SURGERY WITH THE DA VINCI. THE SECOND SURGERY DID NOT HELP AND (B)(6) 2014, I HAD ANOTHER REPAIR. I AM STILL SUFFERING FROM SEVERE INCONTINENCE."
        }
      ],
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      "distributor_zip_code": "",
      "manufacturer_contact_postal_code": "",
      "manufacturer_contact_exchange": "",
      "manufacturer_contact_pcountry": "",
      "suppl_dates_fda_received": ""
    }
  ]
}