BEUDAMED
    FDA Recall Terminated

    0.9% Sodium Chloride Flush Syringe, 2.5 mL. Product Code: E0100-30. Manufactured by Excelsior Medical and distributed by Hospira, Lake Forest, IL under Hospira''s label, Syrex.

    Recall: Z-0044-2007 · Initiated April 24, 2006

    Recall

    Recall Number
    Z-0044-2007
    Event Number
    35960
    Firm
    Excelsior Medical Corp
    FEI Number
    1000122362
    Product Code
    NGT
    Status
    Terminated
    Root Cause
    Other
    Initiated
    April 24, 2006
    Posted
    October 19, 2006
    Terminated
    October 26, 2006
    Address
    1923 Heck Ave, Neptune, NJ, 07753-4428

    Description

    0.9% Sodium Chloride Flush Syringe, 2.5 mL. Product Code: E0100-30. Manufactured by Excelsior Medical and distributed by Hospira, Lake Forest, IL under Hospira''s label, Syrex.

    Reason

    The syringe manufacturer mixed a pre-printed heparin labeled flush syringe with the saline syringes.

    Action

    Excelsior notified Hospira of the recall on 4/24/2006. Hospira notified Morris Dickson and Cardinal Health on 4/28/2006.

    Distribution

    Worldwide.

    Quantity

    466,000 units