BEUDAMED
    FDA Adverse Event Injury Summary report: N

    KENDALL

    MDR report key: 609361 · Received May 23, 2005

    Report

    Report Number
    609361
    Event Type
    Injury
    Date Received
    May 23, 2005
    Date of Event
    May 11, 2004
    Report Date
    May 23, 2005
    Manufacturer
    KENDALL, A DIVISION OF TYCO HEALTHCARE GROUP
    Product Code
    JOW
    Adverse Event
    Yes
    Report Source
    User Facility report
    Reporter Location
    VA, US

    Narratives

    Description of Event or Problem · 1

    WHEN THE SEQUENTIAL COMPRESSION SLEEVES WERE REMOVED FROM THE PATIENT'S LEGS, THERE WAS A 7CM X 4.5CM BLISTER ON THE RIGHT LATERAL ASPECT OF THE CALF.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 KENDALL SCD SEQUENTIAL COMPRESSION SYSTEM JOW KENDALL, A DIVISION OF TYCO HEALTHCARE GROUP 6325 *

    Patients

    Seq Age Sex Outcome Treatment
    1 82 YR Hospitalization| R