D-0009-2022 Class I Terminated
Recall Details
- Product Type
- Drugs
- Report Date
- October 20, 2021
- Initiation Date
- September 24, 2021
- Termination Date
- September 6, 2024
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 19,174 syringes
Product Description
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
Reason for Recall
SUBPOTENT DRUG: Vial contained a liquid substance, instead of the expected powder substance. There was also a lack of full drug effect upon administration.
Distribution Pattern
Nationwide with the USA and Puerto Rico; Canada, Argentina, Costa Rica, Mexico
Code Information
Lot #: D239382D, Exp. Date April 2022