BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    HILL-ROM BASIC CARE BED

    MDR report key: 1785125 · Received July 28, 2010

    Report

    Report Number
    1824206-2010-09054
    Event Type
    Malfunction
    Date Received
    July 28, 2010
    Date of Event
    July 7, 2010
    Report Date
    July 7, 2010
    Manufacturer
    OPTIMAL HEALTHCARE, INC
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Distributor report
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    INFO REC'D INDICATES THAT ALL FOUR SIDERAILS WILL NOT LOCK IN THE UP POSITION. HE IS NOT SURE WHAT IS CAUSING THE ISSUE, BUT BELIEVES THE LATCH GUIDE WAS WELDED TOO FAR FROM THE SIDERAIL LATCHING MECHANISM AND WILL NOT ALLOW THE LATCH BLOCK TO ENGAGE IN THE MECHANISM TO LOCK THE SIDERAIL. THE BED IS LOCATED IN THE ICU, WITH A PT IN THE BED. THE PT WAS NOT INJURED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 HILL-ROM BASIC CARE BED AC POWERED HOSPITAL BED FNL OPTIMAL HEALTHCARE, INC 1440

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK