Reported Jul 8, 2026 · Ongoing

Glucagon Emergency Kit for Low Blood Sugar, Glucagon for Injection USP, 1mg per vial, Diluent for Glucagon, 1 mL…

Lupin Pharmaceuticals Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Lupin Pharmaceuticals Inc. · 5801 Pelican Bay Blvd Ste 500 · Naples, FL · 34108-2734

Is this the product you have?

  • Glucagon Emergency Kit for Low Blood Sugar, Glucagon for Injection USP, 1mg per vial, Diluent for Glucagon, 1 mL syringe, Rx only
  • Manufactured forLupin Pharmaceuticals, Inc., Naples, FL 34108
  • Manufactured byLupin Limited, Nagpur - 441108, INDIA, NDC 70748-311-01
Lot codes and dates
  • 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
Amount recalled
64,894 units

This recall covers 2 products

The agency filed one notice per product. You are reading one of them; the other one is below.

Where it was sold

  • Nationwide

Why it was recalled

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

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA drug enforcement) notice

Data as of Sep 19, 4:18 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.