BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CENTRA BED

    MDR report key: 3223812 · Received July 2, 2013

    Report

    Report Number
    1824206-2013-03315
    Event Type
    Malfunction
    Date Received
    July 2, 2013
    Date of Event
    June 6, 2013
    Report Date
    June 6, 2013
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    KS, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    THE ACCOUNT REPLACED THE BRAKE STEER, BRAKE CASTERS AND THE SPACER BETWEEN THE BRAKE CASTER AND THE BRAKE MECHANISM TO RESOLVE THE ISSUE.

    Description of Event or Problem · 1

    THE ACCOUNT ALLEGED THE BRAKE STEER AND BRAKE CASTERS ARE NOT HOLDING. NO INJURY REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    300531 CENTRA BED A/C POWERED ADJUSTABLE HOSP. BED FNL HILL-ROM, INC. 850

    Patients

    Seq Age Sex Outcome Treatment
    1