{
  "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",
    "results": {
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    {
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          "generic_name": "ENDOSCOPIC INSTRUMENT CONTROL SYSTEM",
          "manufacturer_d_name": "INTUITIVE SURGICAL,INC.",
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          "manufacturer_d_address_2": "",
          "manufacturer_d_city": "SUNNYVALE",
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          "manufacturer_d_zip_code_ext": "",
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          "openfda": {
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            "medical_specialty_description": "Gastroenterology, Urology",
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      "product_problems": [
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      "reporter_state_code": "FL",
      "manufacturer_zip_code": "",
      "suppl_dates_mfr_received": "*;*",
      "mfr_report_type": "FDA Requested",
      "manufacturer_contact_country": "",
      "date_changed": "20250805",
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      "manufacturer_contact_extension": "",
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        {
          "patient_sequence_number": "1",
          "date_received": "20100611",
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            "DA VINCI S SYSTEM INSTRUMENTS & ACCESSORIES"
          ],
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        }
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      "manufacturer_contact_city": "",
      "mdr_report_key": "1721314",
      "removal_correction_number": "",
      "number_devices_in_event": "",
      "date_manufacturer_received": "20100629",
      "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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      "single_use_flag": "",
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      "mdr_text": [
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          "mdr_text_key": "8562052",
          "text_type_code": "Additional Manufacturer Narrative",
          "patient_sequence_number": "1",
          "text": "PRODUCT CODE HAS BEEN REMOVED PER FDA REQUEST."
        },
        {
          "mdr_text_key": "17069730",
          "text_type_code": "Description of Event or Problem",
          "patient_sequence_number": "1",
          "text": "IT WAS REPORTED THAT A PATIENT PASSED AWAY ON (B) (6) 2009, ELEVEN DAYS AFTER UNDERGOING A UROLOGIC PROCEDURE WITH THE DA VINCI S SURGICAL SYSTEM."
        },
        {
          "mdr_text_key": "17234193",
          "text_type_code": "Additional Manufacturer Narrative",
          "patient_sequence_number": "1",
          "text": "ON JUNE 11, 2010, A MESSAGE REQUESTING ADDITIONAL INFORMATION REGARDING THE EVENT WAS LEFT AT THE OFFICE OF THE CONSOLE SURGEON. A FOLLOW-UP MDR WILL BE SUBMITTED IF ADDITIONAL INFORMATION IS RECEIVED."
        }
      ],
      "number_patients_in_event": "",
      "distributor_name": "",
      "manufacturer_g1_address_1": "",
      "distributor_zip_code": "",
      "manufacturer_contact_postal_code": "",
      "manufacturer_contact_exchange": "",
      "manufacturer_contact_pcountry": "",
      "suppl_dates_fda_received": "06/15/2010;07/13/2010"
    }
  ]
}