BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SECURE 2 MED/SURGBED

    MDR report key: 2033364 · Received March 22, 2011

    Report

    Report Number
    1831750-2011-02678
    Event Type
    Malfunction
    Date Received
    March 22, 2011
    Date of Event
    February 22, 2011
    Report Date
    February 22, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    RESULT: FOOTBOARD MODULES.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT SEVERAL MODULES HAD POPPED OUT OF THE FOOTBOARD. IT IS UNK IF THERE WAS PT INVOLVEMENT, HOWEVER, NO ADVERSE CONSEQUENCES WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SECURE 2 MED/SURGBED A/C POWERED HOSPITAL BED FNL STRYKER MEDICAL 3002 NA

    Patients

    Seq Age Sex Outcome Treatment
    1