Baxter Healthcare Corporation recalls CARDENE IV (Nicardipine Hydrochloride) in 0.83% Sodium Chlor
See all recalls from Baxter Healthcare Corporation →Recalled 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.
Hazard / Issue
CGMP Deviations
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Lot # NC177818, Exp Date: 12/31/2026; Lot # NC188869, Exp Date: 12/31/2027.
✅ What Should You Do?
- 1Stop taking this medication and contact your doctor or pharmacist immediately.
- 2Do NOT flush medications down the drain — use an FDA-approved drug take-back program.
- 3Check the lot number on your bottle or packaging against the recalled lots listed above.
- 4Report adverse events to FDA MedWatch or call 1-800-FDA-1088.
Looking for a safe alternative?
Search Amazon for CARDENE IV (Nicardipine Hydrochloride) →If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.
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