BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    REMANUFACTURED BED

    MDR report key: 2944229 · Received January 10, 2013

    Report

    Report Number
    1824206-2013-00270
    Event Type
    Malfunction
    Date Received
    January 10, 2013
    Date of Event
    December 28, 2012
    Report Date
    December 28, 2012
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN REPLACED THE BRAKE CASTERS TO RESOLVE THE ISSUE.

    Description of Event or Problem · 1

    THE TECHNICIAN ALLEGED THAT THE BRAKES ARE SETTING AND HOLDING BUT WOULD SWIVEL WHEN THE BED IS PUSHED FROM THE SIDE. NO PATIENT IMPACT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    14125 REMANUFACTURED BED A/C POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 8500

    Patients

    Seq Age Sex Outcome Treatment
    1