BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    HERCULES MATTRESS

    MDR report key: 24835383 · Received April 9, 2026

    Report

    Report Number
    MW5186644
    Event Type
    Malfunction
    Date Received
    April 9, 2026
    Date of Event
    March 4, 2026
    Report Date
    April 8, 2026
    Manufacturer
    THE MOREL COMPANY
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    SC, US
    Reporter Occupation
    RISK MANAGER
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    NOTED STAINING AND TEARING AFTER UNZIPPING MATTRESS COVERS TO NUMEROUS BEDS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    898924 HERCULES MATTRESS BED, AC-POWERED ADJUSTABLE HOSPITAL FNL THE MOREL COMPANY

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown Other