August 8, 2002
Eli Lilly Has Recalled Glucagon Kit
- The FDA has released the following information.
Glucagon Kit, Glucagon for Injection, USP TROUSSE DE GLUCAGON, 1 mg (1
unit)/vial (with 49 mg Lactose)
(Product #M-8239, DIN 00015377). Recall # D-360-2.
Lots 4ND49M (exp. 12/1/02) and 4ND49N (exp. 3/1/03).
Eli Lilly and Co., Indianapolis, IN, by letter on May 30, 2002.
Firm initiated recall is ongoing.
Subpotent-out of specification result at 12 month time point for potency
(the rat hepatocyte test).
VOLUME OF PRODUCT IN COMMERCE
34,028 UNITS (Lot 4ND49M) and 24,835 UNITS (LOT 4ND49N).