BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GO BED PLUS

    MDR report key: 1963952 · Received January 12, 2011

    Report

    Report Number
    1831750-2011-00385
    Event Type
    Malfunction
    Date Received
    January 12, 2011
    Date of Event
    December 14, 2010
    Report Date
    December 14, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIV.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    ND, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE LOAD CELLS WERE REPLACED. NO PATIENT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GO BED PLUS A/C HOSPITAL BED FNL STRYKER CORP., MEDICAL DIV. 2501 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK