BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GO BED II MED/SURG MED

    MDR report key: 2092300 · Received May 3, 2011

    Report

    Report Number
    1831750-2011-04284
    Event Type
    Malfunction
    Date Received
    May 3, 2011
    Date of Event
    April 8, 2011
    Report Date
    April 8, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CT, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    RESULT: LOAD CEL.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE SCALE WAS NOT WEIGHING PROPERLY. IT IS UNKNOWN IF THERE WAS PATIENT INVOLVEMENT, HOWEVER NO ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GO BED II MED/SURG MED A/C HOSPITAL BED FNL STRYKER MEDICAL FL28C NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK