{
  "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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      "date_changed": "20250812",
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      "manufacturer_contact_extension": "",
      "manufacturer_city": "",
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      "patient": [
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      "event_key": "",
      "manufacturer_g1_country": "",
      "date_report_to_manufacturer": "20120113",
      "manufacturer_contact_city": "",
      "mdr_report_key": "2534528",
      "removal_correction_number": "",
      "number_devices_in_event": "",
      "date_report_to_fda": "20120125",
      "manufacturer_name": "",
      "report_source_code": "User Facility report",
      "remedial_action": [
        ""
      ],
      "manufacturer_g1_zip_code": "",
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      "single_use_flag": "",
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      "mdr_text": [
        {
          "mdr_text_key": "2617677",
          "text_type_code": "Description of Event or Problem",
          "patient_sequence_number": "1",
          "text": "DURING A ROBOTIC ASSISTED MODIFIED RADICAL HYSTERECTOMY AND BILATERAL PARA - AORTIC LYMPHADENECTOMY, THE INSULATING SHEATH ON THE MONOPOLAR SCISSORS MALFUNCTIONED AND LEAKED ELECTRICITY ON TO THE ATHEROSCLEROTIC AORTA. THIS CREATED AN AORTIC TEAR WHICH NECESSITATED CONVERTING TO A LAPAROTOMY AND A VASCULAR SURGEON TO REPAIR THE AORTIC INJURY."
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      "manufacturer_contact_exchange": "",
      "manufacturer_contact_pcountry": "",
      "suppl_dates_fda_received": ""
    }
  ]
}