BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GO BED PLUS

    MDR report key: 1942715 · Received December 10, 2010

    Report

    Report Number
    1831750-2010-04703
    Event Type
    Malfunction
    Date Received
    December 10, 2010
    Date of Event
    November 17, 2010
    Report Date
    November 17, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIVISION
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE BED ALARM AND THE SCALE WERE NOT WORKING PROPERLY. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GO BED PLUS AC POWERED HOSPITAL BED FNL STRYKER CORP., MEDICAL DIVISION 2501 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK