BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    LIKORALL

    MDR report key: 3130542 · Received March 26, 2013

    Report

    Report Number
    1824206-2013-01708
    Event Type
    Malfunction
    Date Received
    March 26, 2013
    Date of Event
    March 1, 2013
    Report Date
    March 4, 2013
    Manufacturer
    LIKO AB
    Product Code
    FSA
    Product Problem
    Yes
    Report Source
    Distributor report
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    COMPLAINT RECORD STATES THAT THE CENTER BOLT THAT CONNECTS THE SLING BAR TO THE STRAP BROKE WITH A PT IN THE SLING. NO INJURY ALLEGED. REFERENCE MFR REPORT # 8030916-2013-00018.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    124811 LIKORALL NON-AC POWERED PATIENT LIFT FSA LIKO AB LIKORALL 242 ES

    Patients

    Seq Age Sex Outcome Treatment
    1