Lupin Pharmaceuticals Inc. recalls Glucagon Emergency Kit for Low Blood Sugar, Glucagon for Injection USP, 1mg per vial, Diluent for Glucagon, 1 mL syringe
Recalled July 8, 2026 · FDA recall D-0723-2026 · Lupin Pharmaceuticals
Hazard
CGMP deviation: OOS result observed for the Gliding Force functionality test during 12-month long term stability testing. · FDA Class II
Units
64,894 units
Sold at
Nationwide within the U.S.
Description
CGMP deviation: OOS result observed for the Gliding Force functionality test during 12-month long term stability testing.
Product
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
Manufacturer(s)
Lupin Pharmaceuticals Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →