Safety Alert 
March 2003

Eli Lilly and Company Has Recalled Humalog Pen  (disposable insulin delivery system)

The Food and Drug Administration (FDA) released the following information.

PRODUCT
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.

CODE
Lot FF2S19C, exp. August 1, 2004.

RECALLING FIRM/MANUFACTURER
Eli Lilly and Company, Indianapolis, IN., by letters dated December 5,
2002. Firm initiated recall ongoing.

REASON
Drug cartridges may be cracked or broken.

VOLUME OF PRODUCT IN COMMERCE
12,825.

DISTRIBUTION
Nationwide.