BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    4 MOTOR ADVANCE BED

    MDR report key: 2100045 · Received May 16, 2011

    Report

    Report Number
    1824206-2011-02725
    Event Type
    Malfunction
    Date Received
    May 16, 2011
    Date of Event
    April 25, 2011
    Report Date
    April 25, 2011
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECH PERFORMED AN ELECTRICAL SAFETY CHECK AND THE READINGS WERE .08 OHMS AND 43UA. THESE READINGS ARE WITHIN SPECS. NO PROBLEMS FOUND.

    Description of Event or Problem · 1

    INFO RECEIVED INDICATES A NURSE ALLEGED BEING SHOCKED BY THE BED. NO INJURIES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 4 MOTOR ADVANCE BED AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 1165

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK