BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PLUM A+

    MDR report key: 382109 · Received March 11, 2002

    Report

    Report Number
    MW1024364
    Event Type
    Malfunction
    Date Received
    March 11, 2002
    Date of Event
    February 14, 2002
    Report Date
    March 11, 2002
    Manufacturer
    ABBOTT LABORATORIES, INC.
    Product Code
    FRN
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MI, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    PT BLOOD PRESSURE DROPPED FROM 88/66 TO 36/30 AFTER 45 MINS. REPLACED PUMP WITH A SYRINGE PUMP AND BLOOD PRESSURE BEGAN TO STABILIZE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PLUM A+ INFUSION PUMP FRN ABBOTT LABORATORIES, INC. PLUM A+ NA

    Patients

    Seq Age Sex Outcome Treatment
    1 *