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FDAFDA · Food and drugs·Recall number D-0390-2024

Nicardipine Hydrochloride Injection (2.5mg/mL), US, 25mg per 10mL, 10mL Vial, Rx only, Distributed by: AuroMedics Pharma LLC 279 Princeton-Hightstown Rd. E. Windsor, NJ 08520 NDC 55150-183-10

Published March 27, 2024 · Recall initiated: February 20, 2024

Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

Failed Impurities/Degradation Specifications: Out of specification for organic impurities

What to do

Voluntary: Firm initiated · Letter

Recall details

Brand
NICARDIPINE HYDROCHLORIDE
Manufacturer
Eugia US LLC
Distributor
Nationwide within the United States
UPC
0355150183012
Lot
Lot #: 3NC23002, Exp. Date 7/24; 3NC22013, 3NC22014, 3NC22015, 3NC22016, 3NC22017, 3NC22018, Exp. Date 2/24; 3NC22020, Exp. Date 3/24
Risk classification
Class II
Area (FDA)
drug
Country
United States

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