BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ACCUMAX MODEL CU2 MATTRESS PUMP

    MDR report key: 2232533 · Received August 26, 2011

    Report

    Report Number
    2232533
    Event Type
    Malfunction
    Date Received
    August 26, 2011
    Date of Event
    August 26, 2011
    Report Date
    August 26, 2011
    Manufacturer
    ENCOMPASS THERAPEUTIC SUPPORT SYSTEMS
    Product Code
    FNM
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    UT, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    ATTEMPTED TO TURN ACCUMAX BED PUMP AND COULD NOT GET IT TO TURN ON. THE BED PUMP WAS SENT TO CLINICAL ENGINEERING AND IT WAS FOUND A LOOSE WIRE ON A CONNECTOR.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ACCUMAX MODEL CU2 MATTRESS PUMP ACCUMAX MATTRESS PUMP FNM ENCOMPASS THERAPEUTIC SUPPORT SYSTEMS * *

    Patients

    Seq Age Sex Outcome Treatment
    1 *