BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CAREASSIST

    MDR report key: 1120087 · Received August 15, 2008

    Report

    Report Number
    9615739-2008-00016
    Event Type
    Malfunction
    Date Received
    August 15, 2008
    Date of Event
    July 16, 2008
    Report Date
    July 16, 2008
    Manufacturer
    HILL-ROM PLUVIGNER
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    THE HOSPITAL PLANT MANAGER REPORTED THAT THE HEAD SECTION RAN UP UNINTENTIONALLY ON THIS BED. HE FOUND A STUCK CAREGIVER HEAD UP SWITCH ON THE RIGHT HEAD SIDERAIL. HE REPLACED THE CAREGIVER MEMBRANE SWITCH LABEL TO RESOLVE THE PROBLEM. HE ALSO STATED THAT THERE WERE NO REPORTED ADVERSE EVENTS ASSOCIATED WITH THIS MALFUNCTION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CAREASSIST AC POWERED HOSPITAL BED FNL HILL-ROM PLUVIGNER 1170 NA

    Patients

    Seq Age Sex Outcome Treatment
    1