BEUDAMED
    FDA Recall Terminated

    Hem-o-lok Endo5 Ligation Applier

    Recall: Z-0031-05 · Initiated August 18, 2004

    Recall

    Recall Number
    Z-0031-05
    Event Number
    30060
    FEI Number
    3005747797
    Product Code
    HBT
    Status
    Terminated
    Root Cause
    Other
    Initiated
    August 18, 2004
    Posted
    October 22, 2004
    Terminated
    January 31, 2005
    Address
    1 Weck Dr., Weck, Research Triangle Park, NC, 27709

    Description

    Hem-o-lok Endo5 Ligation Applier

    Reason

    The jaws may break during clip loading or clip application.

    Action

    Consignees were notified via Federal Express (Domestic) and by email (International and Weck Sales Representatives).

    Distribution

    Nationwide; Australia, Buenos Aires, Canada, France, Korea, New Zealand, Singapore.

    Quantity

    119 units