BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BLOOD PRESSURE CUFF

    MDR report key: 69859 · Received February 19, 1997

    Report

    Report Number
    MW1010750
    Event Type
    Malfunction
    Date Received
    February 19, 1997
    Date of Event
    February 1, 1997
    Report Date
    February 17, 1997
    Manufacturer
    BAXTER HEALTHCARE, INC.
    Product Code
    DXQ
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    TX, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    BLOOD PRESSURE CUFF DOES NOT MAINTAIN PRESSURE WHEN INFUSED NORMALLY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BLOOD PRESSURE CUFF BLOOD PRESSURE CUFF DXQ BAXTER HEALTHCARE, INC. * 6H210980

    Patients

    Seq Age Sex Outcome Treatment
    1 * Other