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Class II · ModerateActive recall

Glucagon

Could cause temporary or reversible harm; serious harm is unlikely.

Does this affect you?
Check your lot numberKit 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.
Where it was soldNationwide within the U.S.
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

CGMP deviation: OOS result observed for the Gliding Force functionality test during 12-month long term stability testing.

What to do

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Made byLupin Limited, Nagpur - 441108, INDIA foreign manufacturer
Brand nameGLUCAGON
Generic nameGLUCAGON
Distributed by / forLupin Pharmaceuticals, Inc., Naples, FL 34108
NDC70748-311-01
Show the full FDA record
Full product labelGlucagon 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
Recalling firmLupin Pharmaceuticals Inc.
DistributionNationwide within the U.S.
Quantity64,894 units
Recall initiated2026-06-23
Report date2026-07-08
Recall completed—
Recall numberD-0723-2026
ClassificationClass II
FDA statusOngoing
Origin on fileNaples FL United States

Related

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Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.