Drug Recall: 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, Manu
Lupin Pharmaceuticals Inc. · June 23, 2026
Reason for Recall
CGMP deviation: OOS result observed for the Gliding Force functionality test during 12-month long term stability testing.
Product Description
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
Distribution
Nationwide within the U.S.
States Affected
NATIONWIDE
Quantity Affected
64,894 units
Source: FDA (openFDA Drug Enforcement)
Recall number: D-0723-2026
Status: ongoing
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