Lupin Pharmaceuticals Inc.: Glucagon Emergency Kit For Low Blood Sugar, Glucagon For Injection Usp, 1mg Per Vial, Diluent For Glucagon
Glucagon Emergency Kit Recall Summary Lupin Pharmaceuticals is recalling Glucagon Emergency Kits (1mg vials with diluent and syringe) distributed nationwide because testing found the syringe's plunger may not move smoothly as required, potentially affecting the kit's ability to deliver the medication properly. The recall affects all states across the U.S. This product is used by people with diabetes to treat severe low blood sugar emergencies.
- Recalling firm
- Lupin Pharmaceuticals Inc.
- 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
- CGMP deviation: OOS result observed for the Gliding Force functionality test during 12-month long term stability testing.
- Category
- drug recall
- Country
- United States
- Agency
- U.S. Food and Drug Administration
- Recall date
- 2026-06-23
- Status
- Ongoing
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- Nationwide within the U.S.
Official recall notice from U.S. Food and Drug Administration
Recall details on Nibble Recalls: https://trynibble.app/recalls/408e0b8d-4338-4de1-968f-741e306ebc88