BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VERSACARE BED

    MDR report key: 2081593 · Received April 13, 2011

    Report

    Report Number
    1824206-2011-02135
    Event Type
    Malfunction
    Date Received
    April 13, 2011
    Date of Event
    March 21, 2011
    Report Date
    March 21, 2011
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN FOUND THE SIDERAIL MOUNTING BRACKET WAS BENT AND THE PIN WAS NOT ENGAGING ALL OF THE WAY. HE STRAIGHTENED THE BRACKET AND REINSTALLED THE BRACKET AND PIN TO REPAIR THE BED.

    Description of Event or Problem · 1

    INFO RECEIVED INDICATES THE RIGHT HEAD SIDE RAIL DOESN'T LATCH IN THE UP POSITION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 VERSACARE BED AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 3200

    Patients

    Seq Age Sex Outcome Treatment
    1