Nicardipine Hydrochloride: 7 recalls on record

Recalled by 1 agency: FDA (7).

First recall on record: July 17, 2013. Most recent: August 26, 2026.

Risk classification: Class II: 6 · Class III: 1

Most recent recalls

DateAgencyProduct
August 26, 2026FDAniCARdipine Hydrochloride Injection, USP, 25 mg/10mL (2.5 mg/mL), packaged in a) 10 mL Si…D-0802-2026
May 7, 2025FDAniCARdipine Hydrochloride Injection, USP, 25 mg/10 mL (2.5 mg/mL), 10 mL Single Dose Vial…D-0398-2025
May 7, 2025FDAniCARdipine Hydrochloride Injection, USP, 25 mg/10 mL (2.5 mg/mL), 10 mL Single Dose Vial…D-0399-2025
May 29, 2024FDAniCARdipine Hydrochloride Injection, USP, 25 mg/10 mL (2.5 mg/mL), 10 x 10 mL Single Dose…D-0503-2024
March 27, 2024FDANicardipine Hydrochloride Injection (2.5mg/mL), US, 25mg per 10mL, 10mL Vial, Rx only, D…D-0390-2024
March 27, 2024FDANicardipine Hydrochloride Injection, USP 25mg/mL (2.5 mg/mL) 10 mL vials, Distributed by:…D-0391-2024
July 17, 2013FDANicardipine Hydrochloride Injection 25 mg/10 mL (2.5 mg/mL), 10 mL single-use vials, Rx O…D-691-2013

Questions about this brand

How many recalls does Nicardipine Hydrochloride have?
Recalert has 7 U.S. recalls on record for Nicardipine Hydrochloride, published between July 17, 2013 and August 26, 2026.
What was the most recent Nicardipine Hydrochloride recall?
FDA recall D-0802-2026, published August 26, 2026: niCARdipine Hydrochloride Injection, USP, 25 mg/10mL (2.5 mg/mL), packaged in a) 10 mL Single Dose Vial (NDC 72572-470-01) and b) 10x10 mL Single Dose Vials (NDC 72572-470-10), Rx Only, Mfd for: Civi…
Which agencies have recalled Nicardipine Hydrochloride products?
Nicardipine Hydrochloride products appear in recalls from: FDA (7).

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