BEUDAMED
    FDA Enforcement Class II Terminated

    M/H MODULAR STEM, Item number 13-104756 - Product Usage: intended for use in limb salvage procedures.

    Recall: Z-0622-2021 · Reported December 23, 2020

    Enforcement

    Recall Number
    Z-0622-2021
    Event ID
    86896
    Classification
    Class II
    Status
    Terminated
    Product Type
    Devices
    Firm
    Biomet, Inc.
    Voluntary / Mandated
    Voluntary: Firm initiated
    Initial Notification
    Letter
    Report Date
    December 23, 2020
    Initiation Date
    November 25, 2020
    Classification Date
    December 17, 2020
    Termination Date
    May 8, 2024
    Address
    56 E Bell Dr, N/A, Warsaw, IN, 46582-6989, United States

    Description

    M/H MODULAR STEM, Item number 13-104756 - Product Usage: intended for use in limb salvage procedures.

    Reason

    Specific lots of multiple sterile medical devices may have a breach in the sterile seal. A breach in the packaging seal could lead to loss of sterility of the device.

    Code Info

    Lot number 832990

    Distribution

    Worldwide distribution. US nationwide, ARGENTINA, AUSTRALIA, Brazil, CANADA, CHILE, CHINA, COSTA RICA, EMEA, HONG KONG, INDIA, JAPAN, KOREA, MALAYSIA, NEW ZEALAND, SINGAPORE, and TAIWAN

    Quantity

    7428