Official recall notice
FDA DrugClass IINotable
Exenatide Injection Recall (Sep 2026) – Amneal Pharmaceuticals
Product: Exenatide 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., Ahmedabad 382213, India; Distributed by: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807, NDC 70121-1685-1
- Recall date
- 2026-09-30
- Category
- Drug
- FDA class
- Class II
Why it was recalled
Hazard
Defective Delivery System: Possibility of no medication in the prefilled pen.
Product description
Defective Delivery System: Possibility of no medication in the prefilled pen.
Affected products
Lot #: AP250095A, Exp 2/28/2027