BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    UNKNOWN STRYKER BOOM MONITOR

    MDR report key: 24114331 · Received January 20, 2026

    Report

    Report Number
    MW5182388
    Event Type
    Malfunction
    Date Received
    January 20, 2026
    Report Date
    January 12, 2026
    Manufacturer
    STRYKER COMMUNICATIONS, INC.
    Product Code
    FQO
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    OTHER
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    (B)(6) (CS) CALLED TO REPORT THAT WHENEVER THE S8 IS CONNECTED TO THE STRYKER BOOM MONITOR VIA HDMI, THE RESOLUTION ON THE STRYKER MONITOR IS GRAINY, AND THE S8 RESOLUTION BECOMES TOO BIG, PUSHING THE RIGHT AND BOTTOM PARTS OF THE MONITOR IMAGE OFF SCREEN. "THIS REPORT REFLECTS INFORMATION RECEIVED BY FDA IN THE FORM OF A NOTIFICATION PER 803.22 (B)(2)".

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    175615 UNKNOWN STRYKER BOOM MONITOR TABLE, OPERATING-ROOM, AC-POWERED FQO STRYKER COMMUNICATIONS, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown