FDA recall D-0399-2025

American Regent, Inc. · Class II · drug

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.

Distribution

Nationwide in the USA

Key facts

Status
Ongoing
Initiation date
2025-04-18
Report date
2025-05-07
Voluntary/Mandated
Voluntary: Firm initiated
Location
New Albany, OH, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0399-2025