{
  "meta": {
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    "terms": "https://open.fda.gov/terms/",
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      "date_manufacturer_received": "20140320",
      "manufacturer_name": "",
      "report_source_code": "Manufacturer report",
      "remedial_action": [
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      "manufacturer_g1_zip_code": "",
      "report_to_manufacturer": "",
      "manufacturer_zip_code_ext": "",
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      "adverse_event_flag": "Y",
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      "mdr_text": [
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          "patient_sequence_number": "1",
          "text": "IT WAS REPORTED THAT DURING A DA VINCI SURGICAL PROCEDURE, THE PATIENT SUSTAINED A COMMON BILE DUCT INJURY. NO OTHER INFORMATION REGARDING THE REPORTED EVENT WAS PROVIDED."
        },
        {
          "mdr_text_key": "11720111",
          "text_type_code": "Additional Manufacturer Narrative",
          "patient_sequence_number": "1",
          "text": "BASED ON THE INFORMATION PROVIDED, INTUITIVE SURGICAL, INC. (ISI) HAS NOT DETERMINED THE ROOT CAUSE FOR THE PATIENT'S INTRA-OPERATIVE COMPLICATION. THERE IS NO REPORT THAT A MALFUNCTION OF A DA VINCI SYSTEM, INSTRUMENT, OR ACCESSORY OCCURRED. ISI HAS MADE SEVERAL FOLLOW-UP ATTEMPTS TO OBTAIN ADDITIONAL INFORMATION CONCERNING THE REPORTED EVENT; HOWEVER, NO ADDITIONAL INFORMATION HAS BEEN RECEIVED. A FOLLOW-UP MEDWATCH REPORT WILL BE SUBMITTED TO THE FDA IF ADDITIONAL INFORMATION IS RECEIVED. BASED ON THE INFORMATION PROVIDED, THIS COMPLAINT IS BEING REPORTED DUE TO THE FOLLOWING CONCLUSION: THE PATIENT SUSTAINED AN INJURY DURING A DA VINCI SURGICAL PROCEDURE."
        }
      ],
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    }
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}