Glucagon Emergency Kit for Low Blood Sugar, Glucagon for Injection, 1 mg per vial…

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

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

What was recalled

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

Recalling firm: Eli Lilly & Company
Origin: IN, United States
Initiated by: Voluntary: Firm initiated
FDA recall number: D-0009-2022

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

Other Glucagon recalls

See all

Class II · Moderate risk Ongoing Jun 23, 2026

Glucagon Emergency Kit for Low Blood Sugar, Glucagon for Injection USP, 1mg per vial, Diluent for Glucagon, 1 mL syringe, Rx…

Reason CGMP deviation: OOS result observed for the Gliding Force functionality test during 12-month long term stability testing.

Lupin Pharmaceuticals Inc. NDC 70748-311-01 D-0723-2026

Class II · Moderate risk Terminated Apr 13, 2022