BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MANUAL BED

    MDR report key: 1623614 · Received February 24, 2010

    Report

    Report Number
    1824206-2010-02986
    Event Type
    Malfunction
    Date Received
    February 24, 2010
    Date of Event
    January 28, 2010
    Report Date
    January 28, 2010
    Manufacturer
    HILL-ROM RITTER
    Product Code
    FNJ
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE ACCOUNT INDICATES THAT THE BRAKE CASTER WAS REPLACED TO REPAIR THE BED.

    Description of Event or Problem · 1

    THE ACCOUNT ALLEGED THAT THE BED MOVED AFTER SETTING THE BRAKES. HE STATED THERE WERE NO INJURIES. HE INDICATED THAT A PT WAS IN THE BED AND THE BED WAS BEING USED IN A PSYCHIATRIC UNIT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MANUAL BED MANUAL HOSPITAL BED FNJ HILL-ROM RITTER 426

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK