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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

Lupin Pharmaceuticals Inc.
Source
FDA
Category
Drugs & Medications
Recall ID
fda-D-0723-2026
Classification
Class II
Recalled
June 23, 2026
Read the official notice

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