BEUDAMED
    FDA Adverse Event Other Summary report: N

    LIKORALL 200

    MDR report key: 2634395 · Received June 20, 2012

    Report

    Report Number
    8030916-2012-00061
    Event Type
    Other
    Date Received
    June 20, 2012
    Date of Event
    March 14, 2012
    Report Date
    May 30, 2012
    Manufacturer
    LIKO AB
    Product Code
    FSA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    A NON HILL-ROM TECH DID AN EVAL OF THE LIFT AND COULD NOT FIND ANY DEFECTS. THE FACILITY HAS STATED THAT THE SLING BAR PROBABLY WAS NOT ATTACHED ACCORDING TO THE INSTRUCTION GUIDE. THE INSTRUCTION GUIDE, 7EN120114-01, STATES: BEFORE LIFTING ALWAYS MAKE SURE THAT THE LIFTING ACCESSORY IS CORRECTLY APPLIED TO THE LIFT.

    Description of Event or Problem · 1

    WHEN TRANSFERRING A PT FROM THE BED TO A SHOWER CHAIR, THE SLING BAR CAME OFF THE LIFT STRAP AND THE PT FELL BACK ONTO THE BED. NO INJURY ALLEGED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LIKORALL 200 NON-AC POWERED PATIENT LIFT FSA LIKO AB 3121001

    Patients

    Seq Age Sex Outcome Treatment
    1 56 YR