BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SECURE 2 MED/SURGBED

    MDR report key: 2022125 · Received March 10, 2011

    Report

    Report Number
    1831750-2011-02317
    Event Type
    Malfunction
    Date Received
    March 10, 2011
    Date of Event
    February 11, 2011
    Report Date
    February 11, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    RESULT: TIMING LINK, MAIN CONTROL MODULE.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE PT HEAD RIGHT SIDERAIL TIMING WOULD NOT LOCK IN THE UP POSITION. IT WAS FURTHER REPORTED THE BED COULD NOT BE MOVED UP OR DOWN. IT IS UNK IF THERE WAS PT INVOLVEMENT OR IF THERE WERE ADVERSE CONSEQUENCES TO REPORT.

    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