Lupin Glucagon Emergency Kit Recall
Glucagon Emergency Kit for Low Blood Sugar, Glucagon for Injection USP, 1mg per vial, Diluent for Glucagon, 1 mL syringe, Rx only, Manufactu
Updated June 23, 2026
Lupin Pharmaceuticals is recalling Glucagon Emergency Kits due to a manufacturing defect that may affect the syringe's ability to inject properly. If you rely on this kit for a low blood sugar emergency, contact your pharmacy or doctor right away for a replacement.
Is the Lupin Pharmaceuticals Inc. recalled? Yes. This product was recalled by FDA on June 23, 2026. Details below.
What is recalled
Glucagon Emergency Kit for Low Blood Sugar, containing Glucagon for Injection USP 1mg per vial, Diluent for Glucagon, and 1 mL syringe. NDC 70748-311-01. Manufactured by Lupin Limited (Nagpur, India) for Lupin Pharmaceuticals Inc. (Naples, FL).
Am I affected
You're affected if you have a Glucagon Emergency Kit with NDC 70748-311-01 dispensed by your pharmacy. Check your kit's label for this number.
What to do right now
Contact your pharmacy or prescribing doctor immediately to get a replacement Glucagon Emergency Kit. Do not use this kit in an emergency until you have confirmed a replacement.
The hazard
CGMP deviation: OOS result observed for the Gliding Force functionality test during 12-month long term stability testing.
Brands affected
- Source
- FDA
- Category
- Drugs & Medications
- Recall ID
- fda-D-0723-2026
- Classification
- Class II
- Recalled
- June 23, 2026
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