BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VERSACARE BED

    MDR report key: 1791216 · Received August 2, 2010

    Report

    Report Number
    1824206-2010-09106
    Event Type
    Malfunction
    Date Received
    August 2, 2010
    Date of Event
    July 8, 2010
    Report Date
    July 8, 2010
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    LA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECH FOUND THE SIDERAIL LATCHING MECHANISM WAS SLUGGISH DUE TO FLUID INGRESS. THE TECH CLEANED THE LATCH MECHANISM TO REPAIR THE BED.

    Description of Event or Problem · 1

    INFO RECEIVED INDICATES THE SIDERAIL IS NOT LATCHING ALL THE TIME.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1