BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    OBGYN TRANSTAR STRETCHER

    MDR report key: 2053490 · Received March 17, 2011

    Report

    Report Number
    1824206-2011-01651
    Event Type
    Malfunction
    Date Received
    March 17, 2011
    Date of Event
    February 21, 2011
    Report Date
    February 21, 2011
    Manufacturer
    HILL-ROM, INC.
    Product Code
    HDD
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    BIOMEDICAL ENGINEER

    Narratives

    Additional Manufacturer Narrative · 1

    THE BIOMED REPLACED THE CASTERS TO REPAIR THE STRETCHER.

    Description of Event or Problem · 1

    THE ACCOUNTS BIOMED ALLEGED THE CASTERS STILL ROTATE AROUND AFTER THE BRAKE IS SET.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 OBGYN TRANSTAR STRETCHER WHEELED STRETCHER HDD HILL-ROM, INC. 8050

    Patients

    Seq Age Sex Outcome Treatment
    1