Glucagon Emergency Kit for Low Blood Sugar recall
Lupin Pharmaceuticals Inc. recalled Glucagon Emergency Kit for Low Blood Sugar on July 8, 2026 because of cGMP deviation: OOS result observed for the Gliding Force functionality test during 12-month long term stability testing. 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.
What's recalled
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
Quantity: 64,894 units
What to do
Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.
Read the official FDA noticeDetails
- Company
- Lupin Pharmaceuticals Inc., Naples, FL
- Date
- Severity
- Class II
the product could cause temporary or reversible health problems. - Where sold
- Nationwide
Nationwide within the U.S. - Status
- Ongoing
- Recall number
- D-0723-2026
- Source
- U.S. Food and Drug Administration
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