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September 29, 2003

Morris Dickson Has Recalled Kaletra Capsules

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

PRODUCT
Kaletra Capsules (lopinavir/ritonavir) capsules, Each soft gelatin capsule contains: Iopinavir 133.3mg, ritonavir 33.3mg, 180 Capsules bottles, Rx only, Abbott Laboratories, North Chicago, IL. Recall # D-320- 3.

CODE
Lot No. 852072E25, Expiration Date June 2004.

RECALLING FIRM/MANUFACTURER
Recalling Firm: Morris Dickson, Shreveport, LA, by telephone on August 1, 2003. Manufacturer: Unknown. Firm initiated recall is ongoing.

REASON
Counterfeit; bottles labeled as containing Kaletra Capsules may contain Kaletra Capsules and/or Agenerase Capsules or a mix of both, as well as, bottles of Kaletra Capsules have been repackaged/relabeled by an unknown source with an extended expiration date/counterfeit lot number.

VOLUME OF PRODUCT IN COMMERCE
58 bottles of 180 capsules.

DISTRIBUTION
Nationwide.

 
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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.