BEUDAMED
    FDA Adverse Event Other Summary report: N

    NBP MODULE

    MDR report key: 232253 · Received July 15, 1999

    Report

    Report Number
    9610816-1999-00003
    Event Type
    Other
    Date Received
    July 15, 1999
    Date of Event
    June 15, 1999
    Report Date
    June 15, 1999
    Manufacturer
    HEWLETT-PACKARD CO.
    Product Code
    DPS
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NE, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THAT THE BLOOD PRESSURE CUFF WAS PLACED ON THE PATIENT'S RIGHT UPPER ARM. THE CUFF WENT UP AND STAYED UP FOR 4 1/2 MINUTES. THE CUFF CAME DOWN WHEN THE STOP BUTTON WAS HIT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 NBP MODULE NBP MODULE DPS HEWLETT-PACKARD CO. M1008B NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA