FDA-Drug2026-07-08Not Yet ClassifiedPROCESSING DEFECT
Lupin Glucagon Emergency Kit recalled for syringe plunger functionality defect
What this means
Lupin Pharmaceuticals is recalling certain lots of its Glucagon Emergency Kit because the syringe plunger may not move smoothly during use. This defect was discovered during stability testing and could prevent the kit from working properly in an emergency.
- Check if your Glucagon Emergency Kit lot number matches one listed in the recall (WB00010, WB00017, WB00019, WB00070, WB00077, WB00078, or WB00130).
- Do not use a recalled kit for treating low blood sugar.
- Contact your pharmacy or healthcare provider for a replacement kit right away.
- Have a backup way to treat severe low blood sugar while waiting for a replacement.
The agency's original wording
Hazard
CGMP deviation: OOS result observed for the Gliding Force functionality test during 12-month long term stability testing.
Intended for
Adults
Illnesses reported
None reported
Sold states
Nationwide within the U.S.
Affected count
64,894 units
Manufactured in
5801 Pelican Bay Blvd Ste 500, N/A, Naples, FL, United States
Products
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
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=99296More Lupin recalls
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