BEUDAMED
    FDA Recall Terminated

    Stryker Trio Mobile Surgery Platform; Model 1033.

    Recall: Z-1155-06 · Initiated May 15, 2006

    Recall

    Recall Number
    Z-1155-06
    Event Number
    35536
    Firm
    Stryker Medical Div. of Stryker Corporation
    FEI Number
    1831750
    Product Code
    FSE
    Status
    Terminated
    Root Cause
    Other
    Initiated
    May 15, 2006
    Posted
    June 17, 2006
    Terminated
    July 4, 2006
    Address
    3800 E. Centre Ave., Portage, MI, 49002

    Description

    Stryker Trio Mobile Surgery Platform; Model 1033.

    Reason

    An incorrect pin may have been used during assembly and therefore the device may give way during use.

    Action

    Consignees were called on 5/15/06 and instructed to discontinue use of these devices until the firm's technician has visited the facility and replaced the pin.

    Distribution

    Worldwide (including USA, Australia, Canada, England, Germany, Italy, Romania and Singapore).

    Quantity

    156