NOW Malaria (Export use only) Item Number 660-430, Kit Number 66005, Kit Number 660-000
FDA Recall Z-0780-04 · Posted 2004-07-20
Recalling FirmBinax, Inc.
Recall StatusTerminated
Product CodeNED
Date Initiated2004-02-18
Date Terminated2004-08-09
Product Quantity555 kits
Reason for Recall
Pouch integrity compromised
Firm Action
Binax initiated the recall on 2/18/04 by telephone or email to customers. European customers were notiified by letter.
Root Cause
Other
Distribution Pattern
KS International: Australia, New Zealand, Japan,Sri-Lanka France, The Netherlands, U.A.E., Oman, S. Africa, Hong Kong, Zimbabwe, India
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.