BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ENDOWRIST

    MDR report key: 24339030 · Received February 13, 2026

    Report

    Report Number
    2955842-2026-04280
    Event Type
    Malfunction
    Date Received
    February 13, 2026
    Date of Event
    September 29, 2025
    Report Date
    May 26, 2026
    Manufacturer
    INTUITIVE SURGICAL, INC
    Product Code
    NAY
    UDI-DI
    00886874119785
    PMA / PMN Number
    K214095
    Removal / Correction Number
    N/A
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IT
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    Narratives

    Additional Manufacturer Narrative · 0

    (B)(4).

    Description of Event or Problem · 0

    3004753838-2026-091154.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    11810 ENDOWRIST PROGRASP FORCEPS NAY INTUITIVE SURGICAL, INC 471093-14 K10241128 0270 00886874119785

    Patients

    Seq Age Sex Outcome Treatment
    1