BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SABINA MOBILE LIFT

    MDR report key: 15492331 · Received September 27, 2022

    Report

    Report Number
    15492331
    Event Type
    Malfunction
    Date Received
    September 27, 2022
    Date of Event
    June 19, 2022
    Report Date
    September 15, 2022
    Manufacturer
    LIKO AB
    Product Code
    FSA
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    CA
    Reporter Occupation
    NURSE
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    THE SABINA LIFT IN THE ED IS MISSING THE CHARGING CABLE AND THE ED IS NOT STOCKED WITH SABINA SLINGS. THIS PREVENTS US FROM BEING ABLE TO SAFELY MOBILIZE BMAT 2 LEVEL PATIENTS IN THE ED. I WILL NOTIFY BIOMED OF THE MISSING CABLE. SLINGS ARE STORED IN THE DEPARTMENT. BIOMED TO REPLACE CORD. BIOMED FIXED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2174331 SABINA MOBILE LIFT LIFT, PATIENT, NON-AC-POWERED FSA LIKO AB SABINA II EE

    Patients

    Seq Age Sex Outcome Treatment
    1 Unknown