November 19, 2003
Walsh Southwest Has Recalled Zyprexa
The FDA has released the following information.
a) Zyprexa Tablets (Olanzapine), 10 mg, 60 tablet bottles,
Rx only. Recall # D-046-4;
b) Zyprexa Tablets (Olanzapine), 15 mg, 60 tablet bottles,
Rx only. Recall # D-047-4.
a) Lot No./Exp Date: 6AH19A (01/05), 7AA39A (03/05), and
b) Lot No./Exp. Date: 6AH35A (01/05) and 6AG70A (11/04).
Walsh Southwest, LLC, San Antonio, TX, by letter dated August 15, 2003. Firm
initiated recall is ongoing.
Counterfeit: An unknown number of bottles bearing these lot numbers are
counterfeit, in that they have been repackaged, relabeled and/or may contain
different strengths or mixed strength tablets differing from their labeled
contents and/or bear extended expiration dates, as the source of the
repacked and/or relabeled bottles is unknown.
VOLUME OF PRODUCT IN COMMERCE