BEUDAMED
    FDA Adverse Event Summary report: N

    HEEL/ELBOW PROTECTOR

    MDR report key: 19018 · Received January 18, 1995

    Report

    Report Number
    MW1004786
    Date Received
    January 18, 1995
    Date of Event
    October 14, 1994
    Report Date
    October 15, 1994
    Manufacturer
    MEDLINE INDUSTRIES, INC.
    Product Code
    FMP
    Report Source
    Voluntary report
    Reporter Location
    NE, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    ACCORDING TO RPTR, LPN WAS USING LIFT TO PLACE PT IN W/C. PT HAD ELBOW PROTECTOR ON RIGHT ELBOW. AFTER SITTING PT IN W/C, SHE NOTED SKIN TEARS ON RIGHT ARM; ONE AREA 5 CM X 2.5 CM AND ANOTHER 4 CM X 2.5 CM. THE TEARS WERE SEEMINGLY CAUSED BY ROUGH EDGES ON ELBOW PROTECTOR. DR NOTIFIED AND BANDAGE-STRIPS APPLIED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 HEEL/ELBOW PROTECTOR HEEL/ELBOW PROTECTOR FMP MEDLINE INDUSTRIES, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1 *