Is Amneal Pharmaceuticals of New York, LLC recalled?

Yes — a recall has been published. Reason: Defective Delivery System: Possibility of no medication in the prefilled pen.

TemporaryFDAOngoing

Can cause harm that is usually temporary. Speak to your pharmacist or doctor — do not stop a prescribed medicine on your own.

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

Check the label for

Lot #: AP250095A, Exp 2/28/2027

Why: Defective Delivery System: Possibility of no medication in the prefilled pen.
Distributed: USA Nationwide
Company: Amneal Pharmaceuticals of New York, LLC
Announced: 30 September 2026This is the date the recall was announced. A company may have started it weeks earlier.
Recall began: 28 August 2026

Already ate or took it and feel unwell? Call Poison Control — 1-800-222-1222

Source: FDA record D-0868-2026 · retrieved 22 September 2026

Every recall is shown word for word from the FDA and USDA, with a link to the source.