BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOLLOS CIRRUS 600 CEILING LIFT

    MDR report key: 20938087 · Received December 16, 2024

    Report

    Report Number
    20938087
    Event Type
    Malfunction
    Date Received
    December 16, 2024
    Date of Event
    December 1, 2024
    Report Date
    December 13, 2024
    Manufacturer
    1073849 ONTARIO LIMITED DBA TOLLOS
    Product Code
    FSA
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    MD
    Reporter Occupation
    RISK MANAGER
    Health Professional
    N

    Narratives

    Description of Event or Problem · 0

    THE IMAGING TECHNOLOGIST AND THE IMAGING TECHNOLOGIST AIDE CORRECTLY CONNECTED THE SLING MAT TO THE TOLLOS CEILING LIFT. THE PATIENT WAS SUCCESSFULLY TRANSFERRED ONTO THE CT TABLE USING THE TOLLOS LIFT. ONCE THE IMAGING WAS COMPLETED, THE SLING WAS CORRECTLY RE-CONNECTED TO THE TOLLOS CEILING LIFT. AS THE PATIENT WAS BEING LIFTING DIRECTLY UP, OFF OF THE CT TABLE THE STRAP BROKE, CAUSING THE PATIENT TO BE DROPPED BACK ONTO THE CT TABLE. THE PATIENT WAS STRUCK IN THE FACE WITH THE METAL LIFT ARM MECHANISM. DUE TO PATIENT¿S COMPLAINT OF NECK PAIN, A CT SCAN OF THE PATIENT¿S CERVICAL SPINE AND FACE WERE COMPLETED ALONG WITH UPRIGHT CERVICAL SPINE FILMS. NO ABNORMAL FINDINGS NOTED. THE PATIENT'S LACERATION ABOVE HER UPPER LIP WAS REPAIRED WITH DERMABOND. THE PATIENT HAD SEVERAL CHIPPED TEETH.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2375007 TOLLOS CIRRUS 600 CEILING LIFT LIFT, PATIENT, NON-AC-POWERED FSA 1073849 ONTARIO LIMITED DBA TOLLOS CIRRUS 600 2253595

    Patients

    Seq Age Sex Outcome Treatment
    1 84 YR Female Other