BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE BED

    MDR report key: 2944285 · Received January 10, 2013

    Report

    Report Number
    1824206-2013-00280
    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
    PA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE HILL-ROM TECH FOUND THERE WAS SOME DEBRIS BUILT UP ON THE SIDERAIL LATCH COMPONENTS. HE CLEANED THE SIDERAIL LATCHING COMPONENTS TO REPAIR THE BED. THE BED FUNCTIONED TO SPECS AFTER HE HAD CLEANED THE LATCHING COMPONENTS.

    Description of Event or Problem · 1

    INFO RECEIVED INDICATED THAT THE RIGHT HEAD SIDERAIL WOULD NOT LATCH.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    14219 TOTALCARE BED AC POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 1900

    Patients

    Seq Age Sex Outcome Treatment
    1