BEUDAMED
    FDA Adverse Event Injury Summary report: N

    RODEOH LLC-COMPRESSION TOP

    MDR report key: 24662490 · Received March 23, 2026

    Report

    Report Number
    MW5185564
    Event Type
    Injury
    Date Received
    March 23, 2026
    Date of Event
    December 31, 2025
    Report Date
    February 18, 2026
    Manufacturer
    RODEOH, LLC
    Product Code
    HEF
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    UNKNOWN
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    THEY ARE SELLING MEDICAL DEVICES, UNREGULATED-COMPRESSION TOPS. MY FRIEND GOT A BLOOD CLOT FROM THEIR PRODUCT, DR BELIEVES THE TIGHTNESS WAS CAUSED FROM PROLONGED USE OF THEIR COMPRESSION TOPS, YET THEY DON'T WARN ANYONE ABOUT THAT. WEBSITE, SOCIAL MEDIA, EMAIL, RETAIL STORE WEBSITE: (B)(6); SOCIAL MEDIA: RODEOHS, EMAIL: (B)(6); THEY ARE SOLD IN MANY STORES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    732326 RODEOH LLC-COMPRESSION TOP BINDER, BREAST HEF RODEOH, LLC

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown