BEUDAMED
    FDA Enforcement Class II Ongoing

    THORACIC ROBOTS, DYNJ908777B

    Recall: Z-1707-2026 · Reported April 8, 2026

    Enforcement

    Recall Number
    Z-1707-2026
    Event ID
    98530
    Classification
    Class II
    Status
    Ongoing
    Product Type
    Devices
    Firm
    Medline Industries, LP
    Voluntary / Mandated
    Voluntary: Firm initiated
    Report Date
    April 8, 2026
    Initiation Date
    February 16, 2026
    Classification Date
    April 1, 2026
    Address
    3 Lakes Dr, Northfield, IL, 60093-2753, United States

    Description

    THORACIC ROBOTS, DYNJ908777B

    Reason

    Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of single use biopsy valves. Potential consequences associated with detachment of fragments from valve include foreign body in patient's tracheobronchial tree, which may require intervention for removal. Other potential consequences include inflammatory response, hypoxia, and prolongation of procedure.

    Code Info

    UDI-DI 10198459269196 (EA) 40198459269197 (CS) LOTS 25EBD732 25GBG733 25IBQ613 25JBD457 25KBT352 26ABA235 26ABP735

    Distribution

    US Nationwide distribution in the states of CA, FL, IL, IN, KY, MA, MD, MT, NY, OH, PA, TN, TX.

    Quantity

    14,379 kits total