BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE

    MDR report key: 2022430 · Received February 16, 2011

    Report

    Report Number
    1824206-2011-00901
    Event Type
    Malfunction
    Date Received
    February 16, 2011
    Date of Event
    February 4, 2011
    Report Date
    February 6, 2011
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Report Source
    Manufacturer report
    Reporter Location
    NJ, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    TECHNICIAN FOUND THAT THE SIDERAIL WOULD NOT LATCH IN UP POSITION. CAUSE: SIDERAIL ASSEMBLY WAS CRACKED. REPLACED THE SIDERAIL ASSEMBLY TO RESOLVE THIS ISSUE.

    Description of Event or Problem · 1

    INFORMATION RECEIVED ALLEGED THAT THE LEFT HEAD SIDERAIL WAS CRACKED AND NOT FUNCTIONING.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TOTALCARE AC POWERED ADJUSTALBE HOSPITAL BED FNL HILL-ROM, INC. PR1840A000002

    Patients

    Seq Age Sex Outcome Treatment
    1