BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CENTRA BED

    MDR report key: 2253412 · Received August 3, 2011

    Report

    Report Number
    1824206-2011-04103
    Event Type
    Malfunction
    Date Received
    August 3, 2011
    Date of Event
    July 18, 2011
    Report Date
    July 18, 2011
    Manufacturer
    HILL-ROM INC
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    VT, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE ACCOUNT'S MAINTENANCE FOUND, WHEN HE UNPLUGGED THE TAPE SWITCHES, THE BED WOULD ALARM EVERY TIME. HE REPLACED THE BED EXIT TAPE SWITCHES TO REPAIR THE BED.

    Description of Event or Problem · 1

    THE ACCOUNT'S MAINTENANCE STATED THAT THE BED EXIT DOESN'T ALARM WHEN THE BED EXIT IS TURNED ON WITH NO ONE IN THE BED. THE RED LED INDICATING BED EXIT POWER DOES TURN ON. NO INJURIES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CENTRA BED AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM INC 1062

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK