US Drug Recall Register
Class II · Moderate risk Terminated Initiated Mar 15, 2011 (15 years ago)

CONCENTRATED SODIUM CHLORIDE INJECTION, USP, 23.4% a) 30 mL SINGLE DOSE VIAL, (NDC…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Presence of Particulate Matter: In the course of inspecting retention samples visual particles were observed.

What was recalled

CONCENTRATED SODIUM CHLORIDE INJECTION, USP, 23.4% a) 30 mL SINGLE DOSE VIAL, (NDC 0517-2930-25), b) 100 mL PHARMACY BULK PACKAGE (NDC 0517-2900-25), Rx Only, AMERICAN REGENT, INC. SHIRLEY, NY 11967.

Recalling firm
Luitpold Pharmaceuticals, Inc.
NDC code
0517-2930-25
Origin
NY, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1378-2012

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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