CARDENE IV (Nicardipine Hydrochloride) in 0.83% Sodium… was recalled on August 6, 2026 in cooperation with the U.S. Food and Drug Administration because CGMP Deviations.
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.
Lot # NC177818, Exp Date: 12/31/2026; Lot # NC188869, Exp Date: 12/31/2027.
Units affected: N/A
Where it was sold: US Nationwide; Puerto Rico; and Chile.
Compare the codes above against the label on your product — usually on the bottom, the back panel, or the packaging. If your unit isn't listed, it is not part of this recall.
CGMP Deviations
Class II means the product might cause a temporary or medically reversible health problem; the chance of serious harm is remote.
Stop using the product. Return it to the place of purchase for a refund, or dispose of it. Contact the recalling firm with questions.
Contact: Recalling firm: Baxter Healthcare Corporation
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Always confirm details on the official notice from the U.S. Food and Drug Administration before acting.
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