BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ZIMMER BROWN DERMATOME

    MDR report key: 50240 · Received September 17, 1996

    Report

    Report Number
    50240
    Event Type
    Malfunction
    Date Received
    September 17, 1996
    Date of Event
    August 14, 1996
    Report Date
    September 13, 1996
    Manufacturer
    ZIMMER PATIENT CARE DIVISION
    Product Code
    GFD
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    MS, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    THE DERMATOME ALLEGEDLY TOOK A FULL THICKNESS SKINGRAFT, EVEN THOUGH IT WAS NOT SET TO TAKE A FULL THICKNESS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ZIMMER BROWN DERMATOME DERMATOME GFD ZIMMER PATIENT CARE DIVISION NA NA

    Patients

    Seq Age Sex Outcome Treatment
    1 23 YR Other