BEUDAMED
    FDA Recall Terminated

    NOW Malaria (Export use only) Item Number 660-430, Kit Number 66005, Kit Number 660-000

    Recall: Z-0780-04 · Initiated February 18, 2004

    Recall

    Recall Number
    Z-0780-04
    Event Number
    28457
    Firm
    Binax, Inc.
    FEI Number
    1221359
    Product Code
    NED
    Status
    Terminated
    Root Cause
    Other
    Initiated
    February 18, 2004
    Posted
    July 20, 2004
    Terminated
    August 9, 2004
    Address
    217 Read St, Portland, ME, 04103-3460

    Description

    NOW Malaria (Export use only) Item Number 660-430, Kit Number 66005, Kit Number 660-000

    Reason

    Pouch integrity compromised

    Action

    Binax initiated the recall on 2/18/04 by telephone or email to customers. European customers were notiified by letter.

    Distribution

    KS International: Australia, New Zealand, Japan,Sri-Lanka France, The Netherlands, U.A.E., Oman, S. Africa, Hong Kong, Zimbabwe, India

    Quantity

    555 kits