Safety Alerts Saves Lives
Safety Alerts  
 
Home Privacy About Us Contact Us Change Preferences
SafetyAlerts
November 19,  2003

Walsh Southwest 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-046-4;
b) Zyprexa Tablets (Olanzapine), 15 mg, 60 tablet bottles,
Rx only. Recall # D-047-4.

CODE
a) Lot No./Exp Date: 6AH19A (01/05), 7AA39A (03/05), and
7EA97A (04/05).
b) Lot No./Exp. Date: 6AH35A (01/05) and 6AG70A (11/04).

RECALLING FIRM/MANUFACTURER
Walsh Southwest, LLC, San Antonio, TX, by letter dated August 15, 2003. Firm initiated recall is ongoing.

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.

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?

Sign-up for SafetyAlerts by Email -
The free internet newsletter that could
some day literally save your life - or
the life of someone you know.

 

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.