BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ZIMMER BIOMET ZDRIVE BATTERY POWERED DRIVER

    MDR report key: 22301026 · Received June 20, 2025

    Report

    Report Number
    MW5171710
    Event Type
    Malfunction
    Date Received
    June 20, 2025
    Date of Event
    June 9, 2025
    Report Date
    June 9, 2025
    Manufacturer
    ZIMMER BIOMET DENTAL CANADA INC.
    Product Code
    FSM
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    NY, US
    Reporter Occupation
    RISK MANAGER
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    TOP BUTTONS WERE STICKING. UNABLE TO OPERATE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    837796 ZIMMER BIOMET ZDRIVE BATTERY POWERED DRIVER TRAY, SURGICAL, INSTRUMENT FSM ZIMMER BIOMET DENTAL CANADA INC. 5094250304

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown