BEUDAMED
    FDA Recall Terminated

    TRIGEN INTERTAN 1.5 NAIL: (1) REF 71676515, 10 MM X 10 CM, 125 degree, LEFT, (2) REF 71676556, 11.5 MM X 36 CM, 125 degree, RIGHT, (3) REF 71676558, 11.5 MM X 38 CM, 125 degree, RIGHT, (4) REF 71676561, 11.5 MM X 42 CM, 125 degree, LEFT, Smith & Nephew, Inc. Orthopedic fixation device.

    Recall: Z-1637-2014 · Initiated April 4, 2014

    Recall

    Recall Number
    Z-1637-2014
    Event Number
    68043
    Firm
    Smith & Nephew Inc
    FEI Number
    1020279
    Product Code
    JDS
    Status
    Terminated
    Root Cause
    Process control
    Initiated
    April 4, 2014
    Posted
    May 20, 2014
    Terminated
    July 1, 2017
    Address
    1450 E. Brooks Rd, Memphis, TN, 38116

    Description

    TRIGEN INTERTAN 1.5 NAIL: (1) REF 71676515, 10 MM X 10 CM, 125 degree, LEFT, (2) REF 71676556, 11.5 MM X 36 CM, 125 degree, RIGHT, (3) REF 71676558, 11.5 MM X 38 CM, 125 degree, RIGHT, (4) REF 71676561, 11.5 MM X 42 CM, 125 degree, LEFT, Smith & Nephew, Inc. Orthopedic fixation device.

    Reason

    A manufacturing error resulted in the set screw being inserted too deep in the affected nails.

    Action

    The firm initiated the recall via an "Urgent - Product Recall 1st Notification - Urgent" letter and e-mail on 04/04/2014, identifying the product, explaining the problem, and the potential risk associated with using the product. Customers are to inspect their inventory, and locate and quarantine any affected product. Additionally, the Inventory Return Certification form should be completed and returned along with any affected product identified, once a Return Authorization number has been obtained from Smith & Nephew's Safety Affairs Department.

    Distribution

    Worldwide Distribution -- USA, France, Germany, Sweden, Switzerland, UK, Canada, Australia, Japan, China, India, Dubai, South Africa, South Korea, Mexico, and Venezuela.

    Quantity

    1,253 units total