November 5, 2003
Rochester Drug Cooperative Has Recalled Zyprexa
The FDA has released the following information.
a) Zyprexa tablets (olanzapine), 5 mg, 60 tablet bottles,
Rx only. Recall # D-014-4;
b) Zyprexa tablets (olanzapine), 10 mg, 60 tablet bottles,
Rx only. Recall D-015-4.
Recalling Firm: Rochester Drug Cooperative Inc., Rochester, NY, by letters
dated September 22, 2003 and September 25, 2003. Firm initiated recall is
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
500 (est) bottles.