BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MAXI MOVE

    MDR report key: 3921512 · Received June 30, 2014

    Report

    Report Number
    3921512
    Event Type
    Malfunction
    Date Received
    June 30, 2014
    Date of Event
    May 13, 2014
    Report Date
    June 25, 2014
    Manufacturer
    ARJO HUNTLEIGH
    Product Code
    FSA
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    MA, US

    Narratives

    Description of Event or Problem · 1

    ARJO LIFT WAS USED IN ICU AND FAILED DURING USE. PATIENT WAS IN UP POSITION. SPARE BATTERY WAS THEN OBTAINED, BUT DID NOT WORK. SPARE BATTERY HAD NOT BEEN CHARGED. PATIENT WAS RELEASED MANUALLY FROM THE LIFT STRAPS. A RECOMMENDED IMPROVEMENT IN THIS TECHNOLOGY IS TO HAVE AN AVAILABLE POWER CORD TO ALLOW OPERATION ON AC POWER. THIS MIGHT PREVENT FUTURE FAILURES WITH A MANUFACTURER MODIFICATION OR OPTION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    379590 MAXI MOVE LIFT, PATIENT, NON-AC-POWERED FSA ARJO HUNTLEIGH MAXI MOVE *

    Patients

    Seq Age Sex Outcome Treatment
    1 *