BEUDAMED
    FDA Recall Terminated

    JUGGERKNOT 2.9MM 2 #2 MB Product Usage: For use in hip arthroplasty

    Recall: Z-0993-2018 · Initiated June 30, 2017

    Recall

    Recall Number
    Z-0993-2018
    Event Number
    79242
    Firm
    Zimmer Biomet, Inc.
    FEI Number
    1825034
    Product Code
    LZO
    Status
    Terminated
    Root Cause
    Packaging process control
    Initiated
    June 30, 2017
    Terminated
    April 13, 2018
    Address
    56 E Bell Dr, Warsaw, IN, 46582-6989

    Description

    JUGGERKNOT 2.9MM 2 #2 MB Product Usage: For use in hip arthroplasty

    Reason

    For soft tissue fixation

    Action

    On June 2, 2017 an URGENT Medical Recall Letter was issued to customers regarding affected product(s). The letter requests customers to review the content and notify affected personnel of the recall. Assist the sales representative in quarantining affected product, which will be removed and returned to recalling firm and then replaced. All customers who may have received product from distributors are to be notified. Questions or concerns can be directed to 1-574-372-4847.

    Distribution

    US in the state of Texas

    Quantity

    50