BEUDAMED
    FDA Recall Terminated

    Arrow central venous catheterization kit, 14 ga x 20 cm

    Recall: Z-0083-04 · Initiated September 16, 2003

    Recall

    Recall Number
    Z-0083-04
    Event Number
    27415
    Firm
    Arrow International Inc
    FEI Number
    3015859709
    Product Code
    KZH
    Status
    Terminated
    Root Cause
    Other
    Initiated
    September 16, 2003
    Posted
    November 1, 2003
    Terminated
    April 5, 2004
    Address
    2400 Bernville Rd, Reading, PA, 19605

    Description

    Arrow central venous catheterization kit, 14 ga x 20 cm

    Reason

    wrong product in box

    Action

    The recalling firm issued a recall letter to their direct customers dated 9/16/03. The recall letter explained the reason for recall and to return the product.

    Distribution

    The products were shipped to distributors in AL, AZ, CA, CO, FL, HI, IL, IN, KS, MD, MI, MN, MO, NC, NM, NY, OH, PA, TN, TX, VA, and WI. The products were shipped to government accounts in AZ, AK, DC, IN, SC, and VA. The products were shipped to hospitals nationwide.

    Quantity

    240 units