BEUDAMED
    FDA Adverse Event Other Summary report: N

    ZIMMER INC

    MDR report key: 279697 · Received May 25, 2000

    Report

    Report Number
    MW1019002
    Event Type
    Other
    Date Received
    May 25, 2000
    Date of Event
    May 15, 2000
    Report Date
    May 16, 2000
    Manufacturer
    ZIMMER, INC.
    Product Code
    KCY
    Report Source
    Voluntary report
    Reporter Location
    MN, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    ZIMMER TOURNIQUET WAS APPLIED TO PT'S THIGH IN USUAL MANNER. AT THE END OF THE PROCEDURE (114 MIN) IT WAS NOTED THAT THE TOURNIQUET CUFF WAS ROLLED AND A ROW OF TINY BLISTERS WAS FOUND WHEN THE CUFF WAS REMOVED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ZIMMER INC TOURNIQUET & CUFF KCY ZIMMER, INC. * 92258100

    Patients

    Seq Age Sex Outcome Treatment
    1 60 YR Other