Recall
FDAHealthJune 23, 2026

Lupin Pharmaceuticals Inc. — 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,

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

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
June 23, 2026

Nationwide within the U.S.

What's affected?

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
UPC
0370748311011
Lot code
WB00010

Additional details

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.

What should I do?

Recommended action

Not Yet Classified recall. Voluntary: Firm initiated Quantity affected: 64,894 units.

View original FDA notice →

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