BEUDAMED
    FDA Adverse Event Other Summary report: N

    3M LITTMANN PEDIATRIC STETHOSCOPE

    MDR report key: 493440 · Received October 31, 2003

    Report

    Report Number
    2110898-2003-00010
    Event Type
    Other
    Date Received
    October 31, 2003
    Date of Event
    August 29, 2003
    Report Date
    September 2, 2003
    Manufacturer
    3M HEALTH CARE
    Product Code
    LDE
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    A CUSTOMER REPORTED THAT A DOCTOR COMPLAINED OF PAIN IN THEIR LEFT EAR AFTER PLACING THE STETHOSCOPE EARTIPS IN THEIR EARS. THE DOCTOR WENT TO THE EMERGENCY ROOM AND WAS DIAGNOSED WITH A LEFT EAR DRUM PERFORATION. A HEARING TEST SHOWED LOSS OF HEARING. THE DOCTOR WILL BE RETESTED IN FOUR WEEKS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 3M LITTMANN PEDIATRIC STETHOSCOPE MANUAL STETHOSCOPE LDE 3M HEALTH CARE NA UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 * Other