BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE BED

    MDR report key: 2914926 · Received December 7, 2012

    Report

    Report Number
    1824206-2012-07997
    Event Type
    Malfunction
    Date Received
    December 7, 2012
    Date of Event
    November 18, 2012
    Report Date
    November 18, 2012
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NC, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    THE HILL-ROM TECH FOUND FOREIGN MATERIAL AROUND THE LATCH PIN CAUSING THE LATCH ARM AND PIN NOT TO LATCH PROPERLY. HE REMOVED LATCHING COMPONENTS IN THE RIGHT INTERMEDIATE SIDERAIL AND CLEANED THEM TO RESOLVE THE ISSUE.

    Description of Event or Problem · 1

    INFORMATION RECEIVED INDICATED THAT THE RIGHT INTERMEDIATE SIDERAIL WOULD NOT LATCH.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1