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SafetyAlerts
November 5,  2003

Midwest Drug Supply Has Recalled Kaletra capsules

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

PRODUCT
Kaletra capsules (lopinavir/ritonavir), 133.3/33.3mg, 180 capsule bottles, Rx Only. Recall # D-029-4.

CODE
Lot No. 852072E25 (Exp. 1JUN2004) and Lot No. 852002E21 (Exp. 12/03 or 02/04).

RECALLING FIRM/MANUFACTURER
Recalling Firm: Midwest Drug Supply LLC by letter via fax on August 25, 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
387 bottles.

DISTRIBUTION
Nationwide
.

 
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Health Professional:

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During 2000 there were over
1050 products recalled in the United
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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.