BEUDAMED
    FDA Adverse Event Other Summary report: N

    VEST

    MDR report key: 661139 · Received January 4, 2006

    Report

    Report Number
    1045510-2006-00002
    Event Type
    Other
    Date Received
    January 4, 2006
    Report Date
    December 5, 2005
    Manufacturer
    HILL-ROM CHARLESTON
    Product Code
    BYI
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AR, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    A PT WAS PRESCRIBED VEST THERAPY BECAUSE OF RECURRENT PNEUMONIA AND CHRONIC ASPIRATION. FOUR MONTHS LATER HIS FAMILY MEMBER STATED THE VEST "MADE HIM WORSE" AND REQUESTED IT BE DISCONTINUED. LARGE AMOUNTS OF SECRETIONS WERE BEING PRODUCED THAT HE WAS UNABLE TO REMOVE WITH COUGHING. A MI-E WAS RCOMMENEDED BUT DECLINED BY THE FAMILY MEMBER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 VEST POWERED PERCUSSOR BYI HILL-ROM CHARLESTON 104 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 10 YR Other