BEUDAMED
    FDA Recall Terminated

    BD Nokor Admix Needle 16 G x 1 TW (1.6mm x 25mm) REF 305216 Sterile BD, Franklin Lakes, NJ MADE IN USA For use in aspiration of medications, typically in the pharmacy setting.

    Recall: Z-2192-2011 · Initiated March 1, 2011

    Recall

    Recall Number
    Z-2192-2011
    Event Number
    58451
    Firm
    Becton Dickinson & Company
    FEI Number
    2243072
    Product Code
    FMI
    Status
    Terminated
    Root Cause
    Packaging
    Initiated
    March 1, 2011
    Posted
    May 13, 2011
    Terminated
    November 30, 2012
    Address
    1 Becton Dr, Franklin Lakes, NJ, 07417-1815

    Description

    BD Nokor Admix Needle 16 G x 1 TW (1.6mm x 25mm) REF 305216 Sterile BD, Franklin Lakes, NJ MADE IN USA For use in aspiration of medications, typically in the pharmacy setting.

    Reason

    Incorrect unit package labels which reflect Reorder #305216 instead of the correct item, Reorder #305213, were used.

    Action

    BD sent an Urgent: Product Recall letter with return response forms to direct consignees on 03/01/11 and 03/02/11 via UPS. The letter identified the affected product and lot along with the reason for the recall. The letter asked customers to complete the enclosed Distributor Packing List and to follow the instructions provided on the Packing List for returning the affected product. The firm will issue a credit upon receipt of the affected product. Customers can contact BD Customer Service if they need assistance or have questions regarding the recall.

    Distribution

    Worldwide Distribution -- USA, including the states of NJ, IL, LA, NM, OH, NV, and VA, and country of Canada.

    Quantity

    161,000 units