BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    OHMEDA MEDICAL

    MDR report key: 355373 · Received October 9, 2001

    Report

    Report Number
    355373
    Event Type
    Malfunction
    Date Received
    October 9, 2001
    Date of Event
    September 26, 2001
    Report Date
    October 3, 2001
    Manufacturer
    OHMEDA INC
    Product Code
    LBI
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    FL, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    WHERE PAD CONNENTS TO HOSE A HARD RIDGE OF GLUE WAS THERE AND PT WAS VERY ACTIVE AND RUBBED FOOT AGAINST RIDGE CAUSING SUPERFICIAL SCRATCHES ON FOOT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    45637 OHMEDA MEDICAL BILI BLANKET PLUS HIGH OUTPUT PHTHER SYS LBI OHMEDA INC HOSPITAL ID#40737 *

    Patients

    Seq Age Sex Outcome Treatment
    1 4 DAY