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Class II · ModerateActive recall

Nicardipine Hydrochloride

Could cause temporary or reversible harm; serious harm is unlikely.

Does this affect you?
Check your lot numberLot #: 25295N0C0, Exp. Date: 04/30/2027.
Where it was soldNationwide within the U.S
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde

What to do

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Made byCivica, Inc.
Brand nameNICARDIPINE HYDROCHLORIDE
Generic nameNICARDIPINE HYDROCHLORIDE
Active ingredient(s)NICARDIPINE HYDROCHLORIDE
Distributed by / forAmerican Regent, Inc.
NDC72572-470-01
Show the full FDA record
Full product labelniCARdipine 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: Civica, Inc., Lehi, UT, Mfd by: American Regent, Inc., New Albany, OH 43054.
Recalling firmAmerican Regent, Inc.
DistributionNationwide within the U.S
Quantity43,460 vials
Recall initiated2026-07-24
Report date2026-08-26
Recall completed—
Recall numberD-0802-2026
ClassificationClass II
FDA statusOngoing
Origin on fileShirley NY United States

Related

Recent drug recallsCheck another medication

Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.