Baxter Healthcare Corporation Recall
CARDENE IV (Nicardipine Hydrochloride) in 0.83% Sodium Chloride Injection, 40 mg in 200 mL (0.2 mg/mL) in GALAXY Single-Dose Container, Manu
Updated August 6, 2026
Baxter Healthcare Corporation is recalling CARDENE IV (Nicardipine Hydrochloride) in 0.83% Sodium Chloride Injection, 40 mg in 200 mL (0.2 mg/mL) in GALAXY Single-Dose Container, Manu. Hazard: CGMP Deviations
Is the Baxter Healthcare Corporation recalled? Yes. This product was recalled by FDA on August 6, 2026. Details below.
What is recalled
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.
Am I affected
You may be affected if you own this product. Check the brand, model, and lot/date codes listed in the recall against your item.
What to do right now
Voluntary: Firm initiated
The hazard
CGMP Deviations
Brands affected
- Source
- FDA
- Category
- Drugs & Medications
- Recall ID
- fda-D-0813-2026
- Classification
- Class II
- Recalled
- August 6, 2026
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