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Medicine / D-0868-2026

U.S. Food and Drug AdministrationD-0868-2026

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…

Class II Distributed nationwide or U.S.-wide Status: Ongoing

What was recalled

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

Recalling firm

Amneal Pharmaceuticals of New York, LLC

Reason for recall

Defective Delivery System: Possibility of no medication in the prefilled pen.

Where it went

USA Nationwide

Shown as U.S. Food and Drug Administration published it (shortened where marked …). Recall Shelf does not change recall facts and is not affiliated with the agency.