BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    8020889-1999-00030

    MDR report key: 257223 · Received December 31, 1999

    Report

    Report Number
    8020889-1999-00030
    Event Type
    Malfunction
    Date Received
    December 31, 1999
    Date of Event
    November 30, 1999
    Report Date
    November 30, 1999
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    VA, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    CUFF POPPED ON INFLATION.

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN