BEUDAMED
    FDA Recall Terminated

    BD 60ml Syringe Luer-Lok tip, Sterile, BD, Franklin Lakes, NJ 07417, Made in USA.

    Recall: Z-1811-2009 · Initiated July 7, 2009

    Recall

    Recall Number
    Z-1811-2009
    Event Number
    52601
    Firm
    Becton Dickinson & Company
    FEI Number
    2243072
    Product Code
    FMF
    Status
    Terminated
    Root Cause
    Packaging process control
    Initiated
    July 7, 2009
    Posted
    August 12, 2009
    Terminated
    October 2, 2009
    Address
    1 Becton Dr, Franklin Lakes, NJ, 07417-1815

    Description

    BD 60ml Syringe Luer-Lok tip, Sterile, BD, Franklin Lakes, NJ 07417, Made in USA.

    Reason

    Insufficient Seal: Becton Dickinson received complaints of insufficient/open seals on one lot of 60 ml Luer-Lok Syringes.

    Action

    Becton Dickinson issued an "Urgent: Product Recall" notice via UPS tracking dated July 7, 2009 to all distributors informing them of the affected product. The firm asked all distributors to identify end customers in an attempt to notify all customers. The firms asks that all affected product be returned. Further questions should be directed to BD Customer Service representatives at 1-888-237-2762.

    Distribution

    Nationwide Distribution -- Including states of IL, CA, VA, PA, and FL.

    Quantity

    133,600 units