FDA-Drug2021-10-20Class I
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
Eli Lilly & Company
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.
Sold states
Nationwide with the USA and Puerto Rico; Canada, Argentina, Costa Rica, Mexico
Affected count
19,174 syringes
Manufactured in
839 S Delaware St, N/A, Indianapolis, IN, United States
Products
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
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0009-2022Don't want to check this manually?
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