BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VERSACARE BED

    MDR report key: 2822022 · Received October 9, 2012

    Report

    Report Number
    1824206-2012-06292
    Event Type
    Malfunction
    Date Received
    October 9, 2012
    Date of Event
    September 19, 2012
    Report Date
    September 19, 2012
    Manufacturer
    HILL-ROM INC
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN FOUND THE COMMUNICATION CABLE WAS NOT SEATED CORRECTLY. THE TECHNICIAN INSTALLED NEW SCREWS AT THE COMMUNICATION CABLE AND SIDECOM BOARD CONNECTION TO RESOLVE THE ISSUE.

    Description of Event or Problem · 1

    THE ACCOUNT ALLEGED THE BED EXIT WAS ALARMING BUT DID NOT SEND A NURSE CALL. NO INJURY REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 VERSACARE BED A/C POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM INC 3200

    Patients

    Seq Age Sex Outcome Treatment
    1