{
  "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": "",
      "manufacturer_contact_t_name": "",
      "manufacturer_contact_state": "CA",
      "manufacturer_link_flag": "Y",
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      "manufacturer_g1_city": "SANTA CLARA",
      "manufacturer_contact_address_1": "3410 CENTRAL EXPRESSWAY",
      "manufacturer_contact_pcity": "40852321",
      "event_type": "Injury",
      "report_number": "2955842-2025-35789",
      "type_of_report": [
        "Initial submission"
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      "product_problem_flag": "N",
      "date_received": "20250827",
      "manufacturer_address_2": "",
      "pma_pmn_number": "K181395",
      "date_of_event": "20250601",
      "reprocessed_and_reused_flag": "N",
      "manufacturer_address_1": "",
      "exemption_number": "",
      "manufacturer_contact_zip_code": "95051",
      "reporter_occupation_code": "NURSE",
      "manufacturer_contact_plocal": "4085232100",
      "noe_summarized": "1",
      "manufacturer_contact_l_name": "NIELSON",
      "source_type": [
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        "User facility"
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      "distributor_zip_code_ext": "",
      "manufacturer_g1_postal_code": "95051",
      "manufacturer_g1_state": "CA",
      "reporter_country_code": "US",
      "manufacturer_contact_area_code": "408",
      "date_added": "20250827",
      "manufacturer_contact_f_name": "IZABEL",
      "device_date_of_manufacturer": "20231027",
      "previous_use_code": "I",
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        {
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          "implant_flag": "",
          "date_removed_flag": "",
          "device_sequence_number": "22807",
          "implant_date_year": "",
          "date_removed_year": "",
          "serviced_by_3rd_party_flag": "",
          "date_received": "20250827",
          "brand_name": "DA VINCI",
          "generic_name": "SEAL",
          "manufacturer_d_name": "INTUITIVE SURGICAL, INC",
          "manufacturer_d_address_1": "3410 CENTRAL EXPRESSWAY",
          "manufacturer_d_address_2": "",
          "manufacturer_d_city": "SANTA CLARA",
          "manufacturer_d_state": "CA",
          "manufacturer_d_zip_code": "95051",
          "manufacturer_d_zip_code_ext": "",
          "manufacturer_d_country": "US",
          "manufacturer_d_postal_code": "95051",
          "device_operator": "HEALTH PROFESSIONAL",
          "model_number": "470500-13",
          "catalog_number": "470500",
          "lot_number": "N/A",
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          "device_availability": "No",
          "device_report_product_code": "GCJ",
          "device_age_text": "",
          "device_evaluated_by_manufacturer": "N",
          "combination_product_flag": "N",
          "udi_di": "",
          "udi_public": "",
          "openfda": {
            "device_name": "Laparoscope, General & Plastic Surgery",
            "medical_specialty_description": "Gastroenterology, Urology",
            "regulation_number": "876.1500",
            "device_class": "2"
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        "Material Fragmentation",
        "Material Fragmentation"
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      "reporter_state_code": "CT",
      "manufacturer_zip_code": "",
      "suppl_dates_mfr_received": "",
      "mfr_report_type": "Initial",
      "manufacturer_contact_country": "US",
      "date_changed": "20251027",
      "health_professional": "Y",
      "summary_report_flag": "N",
      "manufacturer_g1_zip_code_ext": "",
      "manufacturer_contact_extension": "",
      "manufacturer_city": "",
      "manufacturer_contact_phone_number": "4085",
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        {
          "patient_sequence_number": "1",
          "date_received": "20250827",
          "sequence_number_treatment": [
            "DA VINCI INSTRUMENTS AND ACCESSORIES."
          ],
          "sequence_number_outcome": [
            "Required Intervention"
          ],
          "patient_age": "NA",
          "patient_sex": "Male",
          "patient_weight": "",
          "patient_ethnicity": "",
          "patient_race": "",
          "patient_problems": [
            "No Clinical Signs, Symptoms or Conditions",
            "No Clinical Signs, Symptoms or Conditions"
          ]
        }
      ],
      "distributor_city": "",
      "date_report": "20250806",
      "initial_report_to_fda": "Yes",
      "distributor_state": "",
      "event_key": "",
      "manufacturer_g1_country": "US",
      "manufacturer_contact_city": "SANTA CLARA",
      "mdr_report_key": "22907946",
      "removal_correction_number": "N/A",
      "number_devices_in_event": "",
      "date_manufacturer_received": "20250806",
      "manufacturer_name": "",
      "report_source_code": "Manufacturer report",
      "remedial_action": [
        "Other"
      ],
      "manufacturer_g1_zip_code": "95051",
      "report_to_manufacturer": "",
      "manufacturer_zip_code_ext": "",
      "manufacturer_g1_name": "INTUITIVE SURGICAL, INC",
      "adverse_event_flag": "N",
      "distributor_address_1": "",
      "manufacturer_state": "",
      "distributor_address_2": "",
      "manufacturer_postal_code": "",
      "single_use_flag": "Y",
      "manufacturer_country": "",
      "mdr_text": [
        {
          "mdr_text_key": "378703037",
          "text_type_code": "Additional Manufacturer Narrative",
          "patient_sequence_number": "0",
          "text": "INTUITIVE SURGICAL, INC. (ISI) DID NOT RECEIVE THE DA VINCI PRODUCT WITH AN ALLEGED ISSUE TO PERFORM FAILURE ANALYSIS."
        },
        {
          "mdr_text_key": "378703038",
          "text_type_code": "Description of Event or Problem",
          "patient_sequence_number": "0",
          "text": "ON 06-JUN-2025, INTUITIVE SURGICAL, INC. (ISI) RECEIVED MEDWATCH REPORT (MDR) WITH UF/IMPORTER REPORT # (B)(4) STATING: \"PATIENT HERE FOR ROBOTIC PROSTATECTOMY RETROPUBIC RADICAL WITH NERVE SPARING BY DR. [REDACTED]. WHEN SCOPE WAS BEING PLACED THROUGH THE UNIVERSAL SEAL \"TOILET SEAT\" UPON FIRST ENTRY THEY NOTICED A BLACK PIECE OF RUBBER INSIDE THE PATIENT. THE PIECE OF RUBBER WAS REMOVED WITH THE PIECE FULLY INTACT, AND A METHODICAL SWEEP OF THE CAVITY WAS PERFORMED BY THE SURGEON WITH NO OTHER PIECES FOUND. SURGEON CONTINUED THE SURGERY WITHOUT ANY COMPLICATIONS. AFTER THE PROCEDURE THE PIECE OF RUBBER WAS COMPARED TO THE MISSING PIECE UNDER THE UNIVERSAL SEAL AND BOTH PIECES MATCHED WITH NO OTHER MISSING PARTS AND SURGEON CONFIRMED. THE COMPANY WAS NOTIFIED. PER REPORTING CONTACT, \"PER REPORTING CONTACT, THE COMPANY WAS MADE AWARE OF THE ISSUE AND CAME INTO THE HOSPITAL THE NEXT DAY. THERE WAS NO PATIENT HARM, BUT WE CANNOT RETURN TO MFG [MANUFACTURER] BECAUSE THE PRODUCT WAS TOSSED OUT AFTER THE SURGEON EXAMINED THE PRODUCT INTO A SHARPS CONTAINER.\""
        }
      ],
      "number_patients_in_event": "",
      "distributor_name": "",
      "manufacturer_g1_address_1": "3410 CENTRAL EXPRESSWAY",
      "distributor_zip_code": "",
      "manufacturer_contact_postal_code": "95051",
      "manufacturer_contact_exchange": "408",
      "manufacturer_contact_pcountry": "",
      "suppl_dates_fda_received": ""
    }
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}