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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., N…

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

Class II Medicine & devices FDA July 8, 2026 Reached Texas
Read the official FDA notice →

What to do

Stop using the product and check it against the description above. Follow the remedy on the official notice; most recalls are refunded or replaced without a receipt. If you or a family member has already been affected, keep the packaging and the lot code — they're what a claim rests on later.

Details

Recalling company
Lupin Pharmaceuticals Inc. — Naples, FL
Severity
Class II — moderate
Reported
July 8, 2026
Quantity
64,894 units
Recall number
D-0723-2026
Status
Ongoing
Source
FDA

Where it went

Nationwide within the U.S.

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