Drug recall D-0399-2025

Class II Ongoing reported May 7, 2025

Product

niCARdipine Hydrochloride Injection, USP, 25 mg/10 mL (2.5 mg/mL), 10 mL Single Dose Vial, Rx Only, American Regent, Inc., Shirley, NY 11967. NDC carton: 0517-0735-10 / NDC Vial: 0517-0735-01]

Reason for recall

Lack of sterility assurance: Product leakage around the vial neck, which could potentially result in a lack of sterility assurance.

Lots and codes

Lots, expiry: Lot 24086N0C0, 7/31/2025; Lot 24076N0C0, Lot 24090N0C0, 8/31/2025, Lot 25011N0C0, 6/30/2026;

Recall details

Recalling firm
American Regent, Inc., New Albany, OH
Quantity
7,249 (cartons of 10 x 10 mL vials)
Distribution
Nationwide in the USA
Type
Voluntary: Firm initiated
Recall initiated
April 18, 2025

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