FDAFDA · Food and drugs·Recall number D-0009-2022
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
Published October 20, 2021 · Recall initiated: September 24, 2021
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's 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
Voluntary: Firm initiated · Press Release
Recall details
- Manufacturer
- Eli Lilly & Company
- Distributor
- Nationwide with the USA and Puerto Rico; Canada, Argentina, Costa Rica, Mexico
- Lot
- Lot #: D239382D, Exp. Date April 2022
- Risk classification
- Class I
- Area (FDA)
- drug
- Country
- United States
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