BEUDAMED
    FDA Recall Terminated

    Immulite 2500 insulin Kit

    Recall: Z-0324-05 · Initiated November 19, 2004

    Recall

    Recall Number
    Z-0324-05
    Event Number
    30530
    Firm
    Diagnostic Products Corp
    FEI Number
    3005250747
    Product Code
    CFP
    Status
    Terminated
    Root Cause
    Other
    Initiated
    November 19, 2004
    Posted
    December 17, 2004
    Terminated
    March 24, 2005
    Address
    5210 Pacific Concourse Dr, Los Angeles, CA, 90045-6900

    Description

    Immulite 2500 insulin Kit

    Reason

    Low bias of 10 to 40% at different levels of insulin in samples.

    Action

    Customers were notified by telephone on 11/19/2004. They were instructed to discard remaining kits.

    Distribution

    Medical facilities in AK, NY, WI.

    Quantity

    10 kits