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SafetyAlerts
August 6, 2003

Local Repack Has Recalled LIPITOR Tablets

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

PRODUCT
LIPITOR Tablets, (ATORVASTATIN CALCIUM), 20 MG, 90 and 1000 TABLETS bottles, Rx only. Recall # D-284-3.

CODE
Lot 0511022.

RECALLING FIRM/MANUFACTURER
Recalling Firm: Local Repack, Inc., Richton Park, IL, by letters on June 16, 2003.
Manufacturer: Unknown. Firm initiated recall is ongoing.

REASON
Counterfeit product.

VOLUME OF PRODUCT IN COMMERCE
7,189 - 90 tab bottles, 15 - 1000 tab bottles

DISTRIBUTION
Nationwide
.

 
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During 2000 there were over
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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.