Drug recall D-0723-2026

Class II Ongoing reported Jul 8, 2026

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

Reason for recall

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

Lots and codes

Kit Lots: WB00010, Exp. Date Jan 2027; WB00017, WB00019, Exp. Date Feb 2027; WB00070, Exp. Date Jun 2027; WB00077, WB00078, Exp. Date Jul 2027; WB00130, Exp. Date Nov 2027.

Recall details

Recalling firm
Lupin Pharmaceuticals Inc., Naples, FL
Quantity
64,894 units
Distribution
Nationwide within the U.S.
Type
Voluntary: Firm initiated
Recall initiated
June 23, 2026

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