niCARdipine Hydrochloride Injection recall
American Regent, Inc. recalled niCARdipine Hydrochloride Injection on August 26, 2026 because of presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde. It was sold nationwide.
Why it was recalled
Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde
What's recalled
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: Civica, Inc., Lehi, UT, Mfd by: American Regent, Inc., New Albany, OH 43054.
Quantity: 43,460 vials
What to do
Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.
Read the official FDA noticeDetails
- Company
- American Regent, Inc., Shirley, NY
- Date
- Severity
- Class II
the product could cause temporary or reversible health problems. - Where sold
- Nationwide
Nationwide within the U.S - Status
- Ongoing
- Recall number
- D-0802-2026
- Source
- U.S. Food and Drug Administration
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