BEUDAMED
    FDA Recall Terminated

    Catheterization Kits containing Angiographic Syringes with rotator connector.

    Recall: Z-0621-05 · Initiated November 2, 2004

    Recall

    Recall Number
    Z-0621-05
    Event Number
    30478
    Firm
    Hospira Inc.
    FEI Number
    3013319212
    Product Code
    DQO
    Status
    Terminated
    Root Cause
    Other
    Initiated
    November 2, 2004
    Posted
    March 15, 2005
    Terminated
    July 25, 2005
    Address
    275 N Field Dr, Lake Forest, IL, 60045-2579

    Description

    Catheterization Kits containing Angiographic Syringes with rotator connector.

    Reason

    Syringes could possibly allow air to enter the patient's vascular system.

    Action

    Consignees were notified by letter on 11/10/04 or by telephone on 11/11/04.

    Distribution

    Domestic distribution: Nationwide, including 2 military/VA facilities. International distribution: Spain, Belgium, Greece, Japan, and France.

    Quantity

    62080 kits