BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CLINITRON RITEHITE BED

    MDR report key: 3240835 · Received July 16, 2013

    Report

    Report Number
    1824206-2013-03529
    Event Type
    Malfunction
    Date Received
    July 16, 2013
    Date of Event
    June 19, 2013
    Report Date
    June 19, 2013
    Manufacturer
    HILL-ROM, INC.
    Product Code
    INX
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE SERVICE TECHNICIAN REPLACED THE LEFT FOOT BRAKE CASTER TO RESOLVE THE ISSUE.

    Description of Event or Problem · 1

    THE SERVICE TECHNICIAN ALLEGED THE LEFT FOOT BRAKE CASTER IS NOT HOLDING. NO PT IMPACT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    330430 CLINITRON RITEHITE BED BED, AIR FLUIDIZED INX HILL-ROM, INC. 0800

    Patients

    Seq Age Sex Outcome Treatment
    1