BEUDAMED
    FDA Adverse Event Other Summary report: N

    ENTERALITE AMBULATORY ENTERAL FEEDING PUMP

    MDR report key: 1731374 · Received June 16, 2010

    Report

    Report Number
    1722139-2010-00069
    Event Type
    Other
    Date Received
    June 16, 2010
    Date of Event
    April 21, 2010
    Report Date
    June 14, 2010
    Manufacturer
    MOOG MEDICAL DEVICES GROUP
    Product Code
    LZH
    PMA / PMN Number
    K954735
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Description of Event or Problem · 1

    REPORTED BY THE CUSTOMER AS: PUMP HEATS UP WHILE IN BACKPACK TO THE POINT THE FORMULA WARMS UP.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ENTERALITE AMBULATORY ENTERAL FEEDING PUMP LZH MOOG MEDICAL DEVICES GROUP ENTERALITE PUMP

    Patients

    Seq Age Sex Outcome Treatment
    1