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October 29 2003

Walsh Heartland Has Recalled Zyprexa Tablets

(SafetyAlerts) - The FDA has released the following information.

PRODUCT
a) Zyprexa Tablets (Olanzapine), 10 mg, 60 tablet bottles,
Rx only. Recall # D-004-4;
b) Zyprexa Tablets (Olanzapine), 15 mg, 60 tablet bottles,
Rx only. Recall # D-005-4;

CODE
a) Lot Number: 6AA66A;
b) Lot Numbers/Exp. Date: 6AH19A (01/05), 7AA39A (03/05),
and 7EA97A (04/05);
c) Lot Numbers/Exp. Date: 6AH35A (01/05), 6AG70A (11/04);
d) Lot Numbers: 7EC85A and 7AA79A.

RECALLING FIRM
Walsh Heartland, LLC, Paragould, AR, by telephone on August 15, 2003 and August 21, 2003.Firm initiated recall is ongoing.
MANUFACTURER--Unknown

REASON
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
547 bottles.

DISTRIBUTION
Nationwide
.

 
Selected Recent Recalls


Health Professional:

Did you know?
During 2000 there were over
1050 products recalled in the United
States for safety reasons!

How many did you hear about?

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The information contained herein has been obtained from sources that the Company believes to be reliable, however, the Company has not independently verified or confirmed the information and the recipient acknowledges that no representations or warranties are being made in connection with the use of the information.