BEUDAMED
    FDA Adverse Event Injury Summary report: N

    CLINITRON RITE HITE

    MDR report key: 489728 · Received October 17, 2003

    Report

    Report Number
    1045510-2003-00025
    Event Type
    Injury
    Date Received
    October 17, 2003
    Date of Event
    September 19, 2003
    Report Date
    October 16, 2003
    Manufacturer
    HILL-ROM MANUFACTURING, INC.
    Product Code
    INX
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    INVALID DATA

    Narratives

    Description of Event or Problem · 1

    NURSE PULLED ON SIDERAIL TO MOVE BED. SIDERAIL IS REMOVABLE AND WAS UNLOCKED. SIDERAIL CAME OUT AND NURSE FELL. ATTEMPTED TO CONTACT FACILITY NUMEROUS TIMES TO DETERMINE IF CAREGIVER WAS INJURED. ON 10/15/2003 NURSE INFORMED MANUFACTURER THAT FALL HAD RESULTED IN A HERNIATED DISK.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CLINITRON RITE HITE AIR FLUIDIZED THERAPY BED INX HILL-ROM MANUFACTURING, INC. RITE HITE *

    Patients

    Seq Age Sex Outcome Treatment
    1 *