Glucagon Emergency Kit
Lupin recalls Glucagon Emergency Kits due to a stability test failure that may impair emergency use.
Check your kit's NDC 70748-311-01. If affected, stop using the kit and contact Lupin Pharmaceuticals for a replacement or refund.
Why it was recalled
Lupin Pharmaceuticals is recalling Glucagon Emergency Kits (Glucagon for Injection USP, 1 mg per vial, with diluent and syringe) due to a CGMP deviation: an out-of-specification result was observed for the gliding force functionality test during 12-month long-term stability testing, which may affect the device's performance during an emergency.
Is mine affected?
Check the NDC or UPC and strength printed on the package. Yours is affected if it matches one below.
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
| Recall # |
|---|
| N/A |
| D-0723-2026 |
Where it was sold
Distributed nationwide.
Official source
Other recent recalls from Lupin Pharmaceuticals Inc.
Editorial summary by Recall Canary · last updated 2026-07-24 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification