BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VERSACARE BED

    MDR report key: 2024126 · Received March 11, 2011

    Report

    Report Number
    1824206-2011-01450
    Event Type
    Malfunction
    Date Received
    March 11, 2011
    Date of Event
    February 15, 2011
    Report Date
    February 15, 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 LEFT SIDE COILED CABLE WAS WORN THROUGH BY THE CASTER DUE TO THE P-CLIP TURNING TOWARD THE CASTER AND THE CABLE SAGGING. THE COILED CABLE WAS REPLACED TO REPAIR THE BED.

    Description of Event or Problem · 1

    THE ACCOUNT ALLEGED THAT THE CASTER HAS WORN THROUGH THE LEFT COILED CABLE AND THERE ARE BARE WIRES.

    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