BEUDAMED
    FDA Adverse Event Other Summary report: N

    HIL-ROM

    MDR report key: 382103 · Received March 12, 2002

    Report

    Report Number
    1824206-2002-00023
    Event Type
    Other
    Date Received
    March 12, 2002
    Date of Event
    February 12, 2002
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Removal / Correction Number
    1824206-12/18/2001-002C
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    SC, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IN 2002, HOSPITAL REPORTS THAT THE NURSING STAFF ALLEGES THAT THE BED HAD AN UNINTENTIONAL MOVEMENT. SIX DAYS LATER, TSR INSPECTED UNIT BUT COULD NOT DUPLICATE UNINTENTIONAL MOVEMENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 HIL-ROM BED FNL HILL-ROM, INC. 1900 *

    Patients

    Seq Age Sex Outcome Treatment
    1 *