Recall RadarGlucagon 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.
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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