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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…

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

Class II Medicine & devices FDA August 26, 2026 Reached Texas
Read the official FDA notice →

What to do

Stop using the product and check it against the description above. Follow the remedy on the official notice; most recalls are refunded or replaced without a receipt. If you or a family member has already been affected, keep the packaging and the lot code — they're what a claim rests on later.

Details

Recalling company
American Regent, Inc. — Shirley, NY
Severity
Class II — moderate
Reported
August 26, 2026
Quantity
43,460 vials
Recall number
D-0802-2026
Status
Ongoing
Source
FDA

Where it went

Nationwide within the U.S

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