BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ML-4

    MDR report key: 1276407 · Received December 30, 2008

    Report

    Report Number
    9681684-2008-00040
    Event Type
    Injury
    Date Received
    December 30, 2008
    Date of Event
    November 20, 2008
    Report Date
    December 29, 2008
    Manufacturer
    BHM MEDICAL, INC.
    Product Code
    FNG
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    THE FACILITY REPORTED THAT TWO STAFF MEMBERS WERE TRANSFERRING A RESIDENT FROM A WHEELCHAIR TO THE BED. AS THE RESIDENT WAS BEING RAISED FROM THE WHEELCHAIR, THE LEFT SHOULDER STRAP BROKE AND THE RESIDENT FELL BACK INTO THE CHAIR. ANOTHER SLING WAS USED TO GET THE RESIDENT INTO THE BED. NO INJURIES WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ML-4 PATIENT LIFT FNG BHM MEDICAL, INC. 87001001

    Patients

    Seq Age Sex Outcome Treatment
    1