BEUDAMED
    FDA Recall Terminated

    BD Bactec Blood Culture Procedural Tray, Cat. Number 442805 Becton, Dickinson and Company, 7 Loveton Circle, Sparks, MD 21152 Used in conjunction with the blood collection system.

    Recall: Z-3029-2011 · Initiated April 22, 2011

    Recall

    Recall Number
    Z-3029-2011
    Event Number
    59218
    Firm
    Becton Dickinson & Company
    FEI Number
    2243072
    Product Code
    JGE
    Status
    Terminated
    Root Cause
    Device Design
    Initiated
    April 22, 2011
    Posted
    August 16, 2011
    Terminated
    June 6, 2012
    Address
    1 Becton Dr, Franklin Lakes, NJ, 07417-1815

    Description

    BD Bactec Blood Culture Procedural Tray, Cat. Number 442805 Becton, Dickinson and Company, 7 Loveton Circle, Sparks, MD 21152 Used in conjunction with the blood collection system.

    Reason

    BD Vacutainer Push Button Blood Collection Set can potentially undergo cannula separation from the hub.

    Action

    BD Diagnostics sent a "Lot Specific Product Recall" letter dated April 22, 2011 to all affected customers. The letter asked customers return any affected product and provides instructions for its return. The letter ask customers return the attached Packaging List with the shipment. For question on this recall contact BD Diagnostics at (201) 847-5117.

    Distribution

    Nationwide (USA) Distribution.

    Quantity

    34960 units