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SafetyAlerts
April 2, 2003

Eli Lilly and Company Has Recalled Strattera Capsules

(SafetyAlerts) - The Food and Drug Administration (FDA) has released the following information.


PRODUCT
Strattera Capsules (atomoxetine HC1) 40mg, 24 count bottle, Rx only, Adult Sample Pack. Recall # D-188-3.

CODE
6AE95B.

RECALLING FIRM/MANUFACTURER
Eli Lilly and Company, Indianapolis, IN, by fax on January 10, 2003. Firm initiated recall is ongoing.

REASON
Misbranded; bottle label is incorrectly printed as "First use blister".

VOLUME OF PRODUCT IN COMMERCE
89,360 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.