BEUDAMED
    FDA Adverse Event Injury Summary report: N

    SKYTRON PATIENT POSITIONER

    MDR report key: 18858043 · Received March 6, 2024

    Report

    Report Number
    MW5152455
    Event Type
    Injury
    Date Received
    March 6, 2024
    Date of Event
    December 16, 2023
    Report Date
    March 4, 2024
    Manufacturer
    SCHUERCH CORPORATION
    Product Code
    FWZ
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    NURSE
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    WHILE TRANSFERRING THE PATIENT FROM THE BED TO THE OR TABLE THE SKYTRON PATIENT POSITIONER MANUFACTURER # 508-0089 S/N:(B)(6) JUST TORE APART AND THE PATIENT'S FEET WENT STRAIGHT THROUGH THE PADDED POSITIONER STRAIGHT TO THE FLOOR AND THE PATIENT WAS IN A STANDING POSITION. WE ASSISTED THE PATIENT BACK TO THE PATIENT'S BED THAT SHE ARRIVED IN AND GOT ANOTHER SKYTRON PATIENT POSITIONER AND ATTACHED THAT TO THE FOOT OF THE BED. NO PATIENT HARM NOTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    160787 SKYTRON PATIENT POSITIONER OPERATING ROOM ACCESSORIES TABLE TRAY FWZ SCHUERCH CORPORATION 508-0089

    Patients

    Seq Age Sex Outcome Treatment
    1 31 YR Female Required Intervention