BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    POSEY PREEMIE REMOVABLE ID

    MDR report key: 477813 · Received July 22, 2003

    Report

    Report Number
    MW1029274
    Event Type
    Malfunction
    Date Received
    July 22, 2003
    Date of Event
    July 12, 2003
    Report Date
    July 21, 2003
    Manufacturer
    J T POSEY COMPANY
    Product Code
    LDQ
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    OR, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    PREEMIE REMOVABLE "POSEY" I.D. BAND USED ON PT TO LEFT ANKLE. RIGHT FOOT HAD SEVERAL SURFACE SCRATCHES AND 3 DIFFERENT SMALL "PIN-DOT" AREAS OF PUNCTURE, SMEAR OF BLOOD NOTED ON EDGES OF BAND. THE EDGES OF I.D. BAND UNDER WHITE POSEY LABEL NOTED TO BE VERY HARD AND SHARP. NEOSPORIN APPLIED TO FOOT WITHOUT BAND REMOVED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 POSEY PREEMIE REMOVABLE ID REMOVABLE ID BAND LDQ J T POSEY COMPANY 4649 *

    Patients

    Seq Age Sex Outcome Treatment
    1 6 DAY Other