Glucagon Emergency Kit for Low Blood Sugar recall: Subpotent
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…
Why was Glucagon Emergency Kit for Low Blood Sugar 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 should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot #: D239382D, Exp. Date April 2022
- Product
- 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…
- Recalling firm
- Eli Lilly & Company
- Quantity
- 19,174 syringes
- Distribution
- Nationwide with the USA and Puerto Rico; Canada, Argentina, Costa Rica, Mexico
- Recall date
- October 20, 2021
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (drug)