FDAFDA · Food and drugs·Recall number D-0723-2026
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
Published July 8, 2026 · Recall initiated: June 23, 2026
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
CGMP deviation: OOS result observed for the Gliding Force functionality test during 12-month long term stability testing.
What to do
Voluntary: Firm initiated · E-Mail
Recall details
- Brand
- GLUCAGON
- Manufacturer
- Lupin Pharmaceuticals Inc.
- Distributor
- Nationwide within the U.S.
- UPC
- 0370748311011
- Lot
- 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.
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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