BEUDAMED
    FDA Adverse Event Injury Summary report: N

    EZ WAY REGULAR (BASIC) SLING

    MDR report key: 17248204 · Received June 30, 2023

    Report

    Report Number
    MW5119060
    Event Type
    Injury
    Date Received
    June 30, 2023
    Date of Event
    June 21, 2023
    Report Date
    June 28, 2023
    Manufacturer
    EZ WAY, INC.
    Product Code
    IKX
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    IA, US
    Reporter Occupation
    501
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    SLING AND EZ LIFT WERE CONNECTED AND USED APPROPRIATELY AND ACCORDING TO MANUFACTURER GUIDELINES TO LIFT RESIDENT WITH 2 STAFF. RESIDENT WAS WITHIN THE WEIGHT RECOMMENDATION FOR A MEDIUM SLING; HOWEVER, SHE SUDDENLY SHIFTED HER WEIGHT SLIPPED OUT THE SIDE OF THE SLING WHILE IT REMAINED ATTACHED TO THE LIFT STAND.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2040602 EZ WAY REGULAR (BASIC) SLING AID, TRANSFER IKX EZ WAY, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1 103 YR Female Disability