BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CENTRA BED

    MDR report key: 1945959 · Received December 28, 2010

    Report

    Report Number
    1824206-2010-11943
    Event Type
    Malfunction
    Date Received
    December 28, 2010
    Date of Event
    December 8, 2010
    Report Date
    December 8, 2010
    Manufacturer
    HILL-ROM INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NJ, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    ACCOUNT REPLACED THE SIDERAIL CONTROL CABLE THAT WAS CUT TO RESOLVE THE ALLEGED PROBLEM.

    Description of Event or Problem · 1

    ACCOUNT ALLEGED THAT THE SIDERAIL CONTROL CABLE WAS CUT DUE TO THE SLIDING HEAD COVER BEING BENT. ACCOUNT ALLEGED THAT BARE METAL WIRES WERE VISIBLE. THERE WERE NO REPORTED INJURIES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CENTRA BED A/C POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM INC. 852

    Patients

    Seq Age Sex Outcome Treatment
    1