BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    STRYKER SMART ROOM EQUIPMENT MEDIA ROUTER

    MDR report key: 24305098 · Received February 10, 2026

    Report

    Report Number
    MW5183604
    Event Type
    Malfunction
    Date Received
    February 10, 2026
    Date of Event
    January 31, 2026
    Report Date
    February 4, 2026
    Manufacturer
    STRYKER COMMUNICATIONS, INC.
    Product Code
    OCS
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    FL, US
    Reporter Occupation
    RISK MANAGER
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    STRYKER CAMERA WAS NOT SHOWING UP ON MONITORS, CALLED TECH SUPPORT, SWITCH OUT STRYKER BOXES AND STILL COULDN'T GET IT TO WORK. MOVED PATIENT TO A DIFFERENT ROOM TO DO THE SURGERY.

    Description of Event or Problem · 0

    ADDITIONAL INFORMATION RECEIVED ON 3/11/2026 FOR REPORT MW5183604 TO UPDATE MFR.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    371537 STRYKER SMART ROOM EQUIPMENT MEDIA ROUTER ENDOSCOPIC VIDEO IMAGING SYSTEM/COMPONENT, GASTROENTEROLOGY-UROLOGY OCS STRYKER COMMUNICATIONS, INC. INFINITY3

    Patients

    Seq Age Sex Outcome Treatment
    1 53 YR Male Other