BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GREEN CLIP HOUSES

    MDR report key: 24445118 · Received February 25, 2026

    Report

    Report Number
    MW5184409
    Event Type
    Malfunction
    Date Received
    February 25, 2026
    Date of Event
    February 20, 2026
    Report Date
    February 20, 2026
    Manufacturer
    MEDLINE INDUSTRIES, LP - NORTHFIELD
    Product Code
    FZP
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    RISK MANAGER
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    ADDITIONAL INFORMATION RECEIVED ON 04/06/2026 FOR REPORT MW5184409 TO UPDATE MANUFACTURER AND PROCODE. PROCODE: FZP.

    Description of Event or Problem · 0

    GREEN CLIP HOUSES ARE NOT STAYING CLAMPED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    505910 GREEN CLIP HOUSES CLIP, IMPLANTABLE FZP MEDLINE INDUSTRIES, LP - NORTHFIELD MDS6PML 300104813

    Patients

    Seq Age Sex Outcome Treatment
    1 48 YR Female