November 5, 2003
Midwest Drug Supply Has Recalled Kaletra
The FDA has released the following information.
Kaletra capsules (lopinavir/ritonavir), 133.3/33.3mg, 180 capsule bottles,
Rx Only. Recall # D-029-4.
Lot No. 852072E25 (Exp. 1JUN2004) and Lot No. 852002E21 (Exp. 12/03 or
Recalling Firm: Midwest Drug Supply LLC by letter via fax on August 25,
2003. Firm initiated recall is ongoing.
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