Drug recall D-0399-2025
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
Related products
- Nicardipine Hydrochloride – drug information
- NDC 0517-0735 Nicardipine Hydrochloride · Nicardipine Hydrochloride 2.5 mg/mL · American Regent, Inc.