BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CLINITRON RITEHITE BED

    MDR report key: 3221907 · Received July 5, 2013

    Report

    Report Number
    1824206-2013-03343
    Event Type
    Malfunction
    Date Received
    July 5, 2013
    Date of Event
    June 7, 2013
    Report Date
    June 7, 2013
    Manufacturer
    HILL-ROM, INC.
    Product Code
    INX
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    THE SVC TECH FOUND THE ACCOUNT DID NOT HAVE THE BRAKES SET CORRECTLY. THE TECH ADJUSTED THE BRAKES TO RESOLVE THE ISSUE.

    Description of Event or Problem · 1

    THE ACCOUNT ALLEGED THAT THE BEDS BRAKES WERE NOT LOCKING. NO PT IMPACT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    307479 CLINITRON RITEHITE BED BED, AIR FLUIDIZED INX HILL-ROM, INC. 0800

    Patients

    Seq Age Sex Outcome Treatment
    1