June 12, 2002
Pharmacia Corp Has Recalled Lomotil Tablets
- The Food and Drug Administration (FDA) released the following information.
Lomotil tablets, Each tablet contains: diphenoxylate hydrochloride, USP 2.5
mg atropine sulfate USP 0.025 mg, Rx only, bottles of 100, 1,000, 2,500, and
unit dose cartons of 100. Recall # D-286-2.
Lot Numbers C200511 and C200682 in 100 tablet bottles;
Lot Numbers C200195 and C200577 in 1,000 tablet bottles;
Lot Number C200363 in 2,500 tablet bottles;
Lot Number C200360 in 100 tablet unit dose carton.
Recalling Firm: Pharmacia Corp., Kalamazoo, MI, by letters dated May 29,
2002. Firm initiated recall is ongoing.
Tablets may contain metal particles.
VOLUME OF PRODUCT IN COMMERCE
9,720 bottles and cartons.