BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    RESIDENT BED

    MDR report key: 2050172 · Received April 5, 2011

    Report

    Report Number
    1824206-2011-02011
    Event Type
    Malfunction
    Date Received
    April 5, 2011
    Date of Event
    March 8, 2011
    Report Date
    March 8, 2011
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    NO INFO AVAILABLE ON THE REPAIR OF THE BED AT THIS TIME.

    Description of Event or Problem · 1

    ACCOUNT ALLEGED THAT THE POWER CORD WAS CUT AND HAD WIRES SHOWING. NO INJURY REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 RESIDENT BED A/C POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 870

    Patients

    Seq Age Sex Outcome Treatment
    1