BEUDAMED
    FDA Adverse Event Summary report: N

    TOTALCARE-

    MDR report key: 2132239 · Received June 7, 2011

    Report

    Report Number
    1824206-2011-03115
    Date Received
    June 7, 2011
    Date of Event
    May 18, 2011
    Report Date
    May 18, 2011
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    LA, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    TECH FOUND LEFT INTERMEDIATE SIDERAIL WOULD NOT LATCH. REPLACED LATCH KIT TO RESOLVE THIS ISSUE. BED WAS LOCATED IN STORAGE AREA.

    Description of Event or Problem · 1

    INFO PROVIDED INDICATED THAT THE LEFT INTERMEDIATE SIDERAIL WOULD NOT LATCH AUTOMATICALLY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TOTALCARE- AC POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. P1900

    Patients

    Seq Age Sex Outcome Treatment
    1