BEUDAMED
    FDA Adverse Event Injury Summary report: N

    RELIEF BAND

    MDR report key: 258618 · Received January 12, 2000

    Report

    Report Number
    MW1017922
    Event Type
    Injury
    Date Received
    January 12, 2000
    Date of Event
    December 23, 1999
    Report Date
    January 12, 2000
    Manufacturer
    WOODSIDE BIOMEDICAL
    Product Code
    BWK
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MN, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    RAISED RED SKIN IRRITATION FROM THE METAL ON THE WRISTBAND.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 RELIEF BAND ELECTRICAL STIMULATION WRISTBAND BWK WOODSIDE BIOMEDICAL * B9911A3

    Patients

    Seq Age Sex Outcome Treatment
    1 54 YR