BEUDAMED
    FDA Adverse Event Injury Summary report: N

    MINILIFT 160

    MDR report key: 17451727 · Received August 2, 2023

    Report

    Report Number
    MW5120519
    Event Type
    Injury
    Date Received
    August 2, 2023
    Report Date
    July 31, 2023
    Manufacturer
    BRAKO D.O.O
    Product Code
    FSA
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    UK
    Reporter Occupation
    PHYSICIAN
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    A MALE RESIDENT WAS BEING TRANSFERRED FROM THE BED TO A SHOWER CHAIR USING THE HANDICARE MINILIFT 160. AS HE WAS BEING LIFTED TO TRANSFER HIM TO THE SHOWER, CHAIR, HIS FEET SLIPPED OF THE FOOTPLATE OF THE LIFT. THE CARE STAFF TRANSFERRED HIM BACK TO HIS BED. THE RESIDENT BRUISED HIS KNEES DURING THE PROCESS. HE WAS NEVER TAKEN TO THE HOSPITAL, BUT LOOKED OVER BY AMBULANCE STAFF.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    772349 MINILIFT 160 LIFT, PATIENT, NON-AC-POWERED FSA BRAKO D.O.O 60300012

    Patients

    Seq Age Sex Outcome Treatment
    1 Male Other