BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    LIKORALL 240 R2R

    MDR report key: 1971779 · Received January 14, 2011

    Report

    Report Number
    8030916-2010-00085
    Event Type
    Malfunction
    Date Received
    January 14, 2011
    Date of Event
    January 1, 2010
    Report Date
    December 16, 2010
    Manufacturer
    LIKO AB
    Product Code
    FNG
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    DA
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    INFO REC'D INDICATED THAT THE LIFT STRAP CAME OUT OF THE R2R HOOK WHEN COMPLETING A ROOM TO ROOM TRANSFER. NO INJURIES WERE ALLEGED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LIKORALL 240 R2R AC POWERED PATIENT LIFT FNG LIKO AB LIKORALL 240 R2R

    Patients

    Seq Age Sex Outcome Treatment
    1 NA