Drug recall D-0813-2026
Product
CARDENE IV (Nicardipine Hydrochloride) in 0.83% Sodium Chloride Injection, 40 mg in 200 mL (0.2 mg/mL) in GALAXY Single-Dose Container, Manufactured and Marketed by: Baxter Healthcare Corporation, Deerfield, IL 60015 USA, NDC 43066-016-10.
Reason for recall
CGMP Deviations
Lots and codes
Lot # NC177818, Exp Date: 12/31/2026; Lot # NC188869, Exp Date: 12/31/2027.
Recall details
- Recalling firm
- Baxter Healthcare Corporation, Deerfield, IL
- Quantity
- N/A
- Distribution
- US Nationwide; Puerto Rico; and Chile.
- Type
- Voluntary: Firm initiated
- Recall initiated
- August 6, 2026
Related products
- Cardene Iv – drug information
- NDC 43066-009 Cardene Iv · Nicardipine Hydrochloride .1 mg/mL · Baxter Healthcare Corporation
- NDC 43066-016 Cardene Iv · Nicardipine Hydrochloride .2 mg/mL · Baxter Healthcare Corporation