BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    P850 CENTRA BED

    MDR report key: 1171933 · Received September 19, 2008

    Report

    Report Number
    1824206-2008-03529
    Event Type
    Malfunction
    Date Received
    September 19, 2008
    Date of Event
    August 28, 2008
    Report Date
    August 28, 2008
    Manufacturer
    HILL-ROM RITTER
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    UPON COMPLAINT REVIEW, IT WAS DETERMINED THAT THIS TYPE OF FAILURE HAS THE POTENTIAL TO CAUSE SERIOUS INJURY. THE TECHNICIAN REPLACED THE POWER CORD IN ORDER TO RESOLVE THE PROBLEM.

    Description of Event or Problem · 1

    WHILE CONDUCTING MAINTENANCE, A TECHNICIAN DISCOVERED THAT THE POWER CORD ON THIS BED HAS LOST THE GROUND, THE PLUG, AND WAS NOT PROPERLY GROUNDED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 P850 CENTRA BED AC POWERED HOSPITAL BED FNL HILL-ROM RITTER P850 NA

    Patients

    Seq Age Sex Outcome Treatment
    1