FDASeptember 24, 2021drug
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 recall recorded by the U.S. Food & Drug Administration.
The 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.
What to do
FDA enforcement status: Terminated
Brands named
eli lillyelieli lilly
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
- FDAWegmans Ultimate Plain Cheesecake Large Net Wt 3.13 lb (1.42kg), shrink wrapped in a collar, 8 cakes per wholesale case2025-09-29
- FDASterile Diluent, HUMALOG U-100 (insulin lispro injection), HUMULIN R U-100 REGULAR (insulin human injection), Insulin Lispro Injection u-100, 10 mL, Use ONLY with Insulins listed on carton, Marketed by: Lilly USA, LLC, Indianapolis, IN 46285. NDC: 0002-0800-012024-03-12
- FDATrulicity (dulaglutide), 0.75 mg/0.5 mL, 4 Single-Dose Pens per box, Rx only, Eli Lilly and Company, Indianapolis, IN 46285, NDC 0002-1433-802021-08-19
- FDAZyprexa Intramuscular, Olanzapine for Injection, 10 MG per Single Use Vial, Rx only, Marketed by: Lilly USA, LLC, Indianapolis, IN 46285, NDC# 0002-7597-012021-06-29
- CPSCLilly of New York Children's Winter Boots Recalled by Kidz Concepts Due to Violation of Federal Lead Content Ban; Sold Exclusively at Zulily.com (Recall Alert)2020-03-19
- FDAERBITUX CETUXIMAB Injection, 200 mg/100 mL (2 mg/mL), 100 mL per single-use vial, Rx only, Manufactured by: ImClone LLC, a wholly-owned subsidiary of Eli Lilly and Company, Branchburg, NJ 08876 USA. NDC: 66733-958-232018-11-08
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