BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    *

    MDR report key: 2250775 · Received August 28, 2011

    Report

    Report Number
    2250775
    Event Type
    Malfunction
    Date Received
    August 28, 2011
    Date of Event
    August 3, 2011
    Report Date
    August 28, 2011
    Manufacturer
    KINETIC CONCEPTS, INC.
    Product Code
    OMP
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    MI, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    WOUND VAC PUMP RUNNING OFF BATTERY POWER EVEN WITH THE POWER CORD PLUGGED IN. BATTERY WAS NOT CHARGING WITH THE POWER CORD PLUGGED IN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * NEGATIVE PRESSURE WOUND THERAPY SYSTEM OMP KINETIC CONCEPTS, INC. 60090 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 52 YR