BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 1964525 · Received December 22, 2010

    Report

    Report Number
    1824206-2010-11905
    Event Type
    Malfunction
    Date Received
    December 22, 2010
    Date of Event
    December 6, 2010
    Report Date
    December 6, 2010
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    ME, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN FOUND THE TEETH ON THE CASTERS WERE WORN. THE TECHNICIAN REPLACED THE CASTERS TO REPAIR THE BED.

    Description of Event or Problem · 1

    INFO REC'D INDICATES THE BRAKES WILL NOT HOLD. THE CASTER BRAKES HOLD BUT THEY ARE NOT LOCKING THE CASTER TEETH AND ALLOWING THE CASTER TO SWIVEL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TRANSTAR STRETCHER WHEELED STRETCHER FPO HILL-ROM, INC. 8000

    Patients

    Seq Age Sex Outcome Treatment
    1