BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ADVANCE BED

    MDR report key: 2020103 · Received March 10, 2011

    Report

    Report Number
    1824206-2011-01429
    Event Type
    Malfunction
    Date Received
    March 10, 2011
    Date of Event
    April 6, 2008
    Report Date
    April 6, 2008
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    DE, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE ACCOUNT DISASSEMBLED THE HI/LOW BRAKE ASSEMBLY AND CLEANED AND DEGREASED THE HI/LOW BRAKE ASSEMBLY TO RESOLVE THE ISSUE. THIS MDR IS A RESULT OF CAPA ACTIVITY FOR THE RETROSPECTIVE REVIEW OF COMPLAINTS.

    Description of Event or Problem · 1

    ACCOUNT ALLEGED THAT THE BED HAD A HI/LOW DRIFT PROBLEM. NO INJURY REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ADVANCE BED A/C POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 1130

    Patients

    Seq Age Sex Outcome Treatment
    1