American Regent recalls niCARd: 25 mg/10mL injection vials contaminated with hair, glass, or paraformaldehyde. Product may cause serious injury if injected. Contact for return instructions.
Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde
American Regent is recalling niCARdipine Hydrochloride Injection vials that contain hair, glass, or paraformaldehyde particles. This contamination could cause serious injury if injected.
The injection vials contain hair, glass, or paraformaldehyde particles. These contaminants could cause serious injury if injected into the body, such as tissue damage or infection.
People who have the recalled niCARdipine Hydrochloride Injection vials (NDC 72572-470-01 or 72572-470-10) for medical use. Healthcare providers and patients using this medication are at risk.
Check for vials labeled 'niCARdipine Hydrochloride Injection, USP, 25 mg/10mL (2.5 mg/mL)' with NDC numbers 72572-470-01 or 72572-470-10. These were manufactured for Civica, Inc. in Lehi, UT and distributed by American Regent, Inc. in New Albany, OH.
Immediately discard the recalled niCARdipine Hydrochloride Injection vials if you have them.
The vials contain hair, glass, or paraformaldehyde particles that could cause serious injury if injected.
Check for vials labeled 'niCARdipine Hydrochloride Injection, USP, 25 mg/10mL (2.5 mg/mL)' with NDC numbers 72572-470-01 or 72572-470-10.
Immediately discard the vials and contact American Regent, Inc. for further instructions.
We’ve drafted a message you can send American Regent to request your refund or repair — edit it as you like.
Subject: Recall D-0802-2026 — American Regent American Regent Hello, I own a American Regent that is covered by recall D-0802-2026 from American Regent. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
