Drug recall D-0723-2026
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
Related products
- Glucagon – drug information
- NDC 70748-311 Glucagon · · Lupin Pharmaceuticals, Inc.