BEUDAMED
    FDA Adverse Event Injury Summary report: N

    SOCLEAN 3

    MDR report key: 24800257 · Received April 7, 2026

    Report

    Report Number
    MW5186422
    Event Type
    Injury
    Date Received
    April 7, 2026
    Report Date
    April 2, 2026
    Manufacturer
    SOCLEAN, INC.
    Product Code
    QXQ
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    VA, US
    Reporter Occupation
    PATIENT
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    EXCESS FLUIDS IN MY LUNGS PROBLEMS BREATHING. I DON'T HAVE SPECIFIC DATES BUT SEE DOCTOR'S REGULARLY. PT CODE-2010. DEVICE CODE-2993. REFERENCED REPORTS-MW5186421.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    872363 SOCLEAN 3 RESPIRATORY ACCESSORY MICROBIAL REDUCTION DEVICE. QXQ SOCLEAN, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1 61 YR Male Disability