BEUDAMED
    FDA Recall Terminated

    StayFuse PROX 03.3 MM sterile intramedullary bone screw distributed by Zimmer

    Recall: Z-0948-03 · Initiated May 28, 2003

    Recall

    Recall Number
    Z-0948-03
    Event Number
    26405
    Firm
    Pioneer Surgical Technology
    FEI Number
    1000115331
    Product Code
    HWC
    Status
    Terminated
    Root Cause
    Other
    Initiated
    May 28, 2003
    Posted
    June 21, 2003
    Terminated
    September 12, 2003
    Address
    375 River Park Circle, Marquette, MI, 49855

    Description

    StayFuse PROX 03.3 MM sterile intramedullary bone screw distributed by Zimmer

    Reason

    Label may bear an incorrect part number [2227-02-02] and size [03.8MM].

    Action

    A recall letter dated 5/28/03 was sent to the sole distributor, asking them to recall from their customers.

    Distribution

    Indiana

    Quantity

    159