BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ELECTRIC MED/SURG BED

    MDR report key: 2012883 · Received March 3, 2011

    Report

    Report Number
    1831750-2011-02147
    Event Type
    Malfunction
    Date Received
    March 3, 2011
    Date of Event
    February 3, 2011
    Report Date
    February 3, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IL, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    WELD.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE HAND WELD IS BROKEN. IT IS UNK IF THERE WAS PT INVOLVEMENT OR IF THERE ARE ADVERSE CONSEQUENCES TO REPORT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ELECTRIC MED/SURG BED AC HOSPITAL BED FNL STRYKER MEDICAL FL23E NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK