BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE

    MDR report key: 1934273 · Received December 3, 2010

    Report

    Report Number
    1824206-2010-11384
    Event Type
    Malfunction
    Date Received
    December 3, 2010
    Date of Event
    November 9, 2010
    Report Date
    November 9, 2010
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    KY, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECH FOUND BUILD UP IN THE SIDE RAIL LATCH MECHANISM CAUSING THE PROBLEM. THE TECH CLEANED THE SIDE RAIL LATCH ASSEMBLY AND REPLACED A BROKEN CENTER ARM COVER TO REPAIR THE BED.

    Description of Event or Problem · 1

    INFO REC'D INDICATES THE RIGHT INTERMEDIATE SIDE RAIL WOULD NOT LATCH.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TOTALCARE AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 1900

    Patients

    Seq Age Sex Outcome Treatment
    1