BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    RESIDENT BED

    MDR report key: 1934280 · Received December 3, 2010

    Report

    Report Number
    1824206-2010-11375
    Event Type
    Malfunction
    Date Received
    December 3, 2010
    Date of Event
    November 8, 2010
    Report Date
    November 8, 2010
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE ACCOUNT ISOLATED THE PENDANT AND THE LOCKOUT BOX. AFTER TROUBLESHOOTING, THE ACCOUNT FOUND THAT THE CONTROL BOX WAS BAD. THE ACCOUNT REPLACED THE CONTROL BOX TO CORRECT THE ISSUE.

    Description of Event or Problem · 1

    THE ACCOUNT STATED THAT THE HEAD OF THE BED WILL NOT LOWER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 RESIDENT BED AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 870

    Patients

    Seq Age Sex Outcome Treatment
    1