US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Jun 23, 2026 (2 months ago)

Glucagon Emergency Kit for Low Blood Sugar, Glucagon for Injection USP, 1mg per vial…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

CGMP deviation: OOS result observed for the Gliding Force functionality test during 12-month long term stability testing.

What was recalled

Glucagon Emergency Kit for Low Blood Sugar, Glucagon for Injection USP, 1mg per vial, Diluent for Glucagon, 1 mL syringe, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Naples, FL 34108, Manufactured by: Lupin Limited, Nagpur - 441108, INDIA, NDC 70748-311-01

Recalling firm
Lupin Pharmaceuticals Inc.
NDC code
70748-311-01
Origin
FL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0723-2026

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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