November 5, 2003
Mid Atlantic Csc Has Recalled Kaletra Capsules
The FDA has released the following information.
Kaletra Capsules (Ritonavir/Lopinavir 33.3mg/133.3mg), 180 capsule bottles,
Rx only. Recall # D-018-4.
Lot 852002E21, EXP 1 FEB 2004.
Recalling Firm: Mid Atlantic Csc, Perryman, MD, by e-mail on September 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