March 05, 2003
Eli Lilly and Company Has Recalled
The Food and Drug
Administration (FDA) released the following information.
Humalog Pen (insulin lispro injection, rDNA origin), U-100, 3 mL, 100
units per mL, disposable insulin delivery system. Rx only, NDC 0002-8725-
01 (HP-8725). Recall # D-112-3.
Lot FF2S19C, exp. August 1, 2004.
Eli Lilly and Company, Indianapolis, IN., by letters dated December 5,
2002. Firm initiated recall ongoing.
Drug cartridges may be cracked or broken.
VOLUME OF PRODUCT IN COMMERCE