BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VERSACARE

    MDR report key: 1171952 · Received September 19, 2008

    Report

    Report Number
    1824206-2008-03504
    Event Type
    Malfunction
    Date Received
    September 19, 2008
    Date of Event
    August 29, 2008
    Report Date
    August 29, 2008
    Manufacturer
    HILL-ROM RITTER
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    DENNIS MUNOZ REPORTED THAT THE PATIENT PENDANT WOULD NOT PLACE A NURSE CALL. REPORTER REPORTED THAT THE PATIENT PENDANT DID NOT LOOK DAMAGED. HE REPLACED THE PATIENT PENDANT, AND THIS RESOLVED THE ISSUE.

    Description of Event or Problem · 1

    HILL-ROM TECHNICAL SERVICE REPRESENTATIVE WAS PERFORMING PREVENTIVE MAINTENANCE WHEN HE DISCOVERED THAT THERE WAS NO NURSE CALL. THERE WERE NO REPORTED INJURIES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 VERSACARE AC POWERED HOSPITAL BED FNL HILL-ROM RITTER P3200 NA

    Patients

    Seq Age Sex Outcome Treatment
    1