Recall RadarExenatide Injection, USP, 250 mcg/mL, 1.2 mL per prefilled pen, Rx Only, Subcutaneous Use Only, For Single Patient Use Only, Manufactured by: Amneal Pharmaceuticals Pvt. Ltd., Ahm…
Defective Delivery System: Possibility of no medication in the prefilled pen.
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
- Amneal Pharmaceuticals of New York, LLC — Brookhaven, NY
- Severity
- Class II — moderate
- Reported
- September 30, 2026
- Quantity
- 5,694 pens
- Recall number
- D-0868-2026
- Status
- Ongoing
- Source
- FDA
Where it went
USA Nationwide
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