BEUDAMED
    FDA Enforcement Class II Terminated

    ZVplasty Directional Cement Cannula (4 pieces per pack), REF VCF-1080-S4. For use in Orthopedic / spinal procedures.

    Recall: Z-1726-2021 · Reported June 9, 2021

    Enforcement

    Recall Number
    Z-1726-2021
    Event ID
    87661
    Classification
    Class II
    Status
    Terminated
    Product Type
    Devices
    Firm
    Zavation
    Voluntary / Mandated
    Voluntary: Firm initiated
    Initial Notification
    E-Mail
    Report Date
    June 9, 2021
    Initiation Date
    March 25, 2021
    Classification Date
    June 1, 2021
    Termination Date
    March 20, 2023
    Address
    220 Lakeland Pkwy, Flowood, MS, 39232-9552, United States

    Description

    ZVplasty Directional Cement Cannula (4 pieces per pack), REF VCF-1080-S4. For use in Orthopedic / spinal procedures.

    Reason

    Products distributed as sterile may not have been adequately sterilized

    Code Info

    Lot: 20061366

    Distribution

    US nationwide distribution.

    Quantity

    11 units