Eli Lilly & Company recalls Glucagon Emergency Kit for Low Blood Sugar, Glucagon for Injection, 1 mg per vial; Diluent for Glucagon, 1 mL syringe. R

Recalled October 20, 2021 · FDA recall D-0009-2022 · Eli Lilly &

Hazard

SUBPOTENT DRUG: Vial contained a liquid substance, instead of the expected powder substance. There was also a lack of full drug effect upon administration. · FDA Class I

Units

19,174 syringes

Sold at

Nationwide with the USA and Puerto Rico; Canada, Argentina, Costa Rica, Mexico

Description

SUBPOTENT DRUG: Vial contained a liquid substance, instead of the expected powder substance. There was also a lack of full drug effect upon administration.

Product

Glucagon Emergency Kit for Low Blood Sugar, Glucagon for Injection, 1 mg per vial; Diluent for Glucagon, 1 mL syringe. Rx only, Marketed by: Lilly USA, LLC, Indianapolis, IN 46285; Glucagon, NDC: 0002-8031-01

Manufacturer(s)

Eli Lilly & Company

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →