FDA Media Alert Detail

Drug Recall

FDA Drug Recall: CONCENTRATED SODIUM CHLORIDE INJECTION, USP, 23.4% a) 30 mL SINGLE DOSE VIAL, (NDC 0517-2930-25),...

  • U.S. Food and Drug Administration
  • June 20, 2012
  • ID: D-1378-2012

Drug Enforcement Report Details

Recall NumberD-1378-2012
Recalling FirmLuitpold Pharmaceuticals, Inc.
ClassificationClass II
Voluntary / MandatedVoluntary: Firm initiated
Distribution PatternNationwide, Puerto Rico, and Abu Dhabi
StatusTerminated
Product Description

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.

Reason for Recall

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

Code Information

30 mL Lots: 9198, 9252, 9299, 9305, 9402, 9423, 9432, 9553, 9595, 9646, 9681, 9737, 9797, 9831, 0051, 0095, 0362; 100 mL Lots: 9225, 9492, 9711, 0007, 0058


Content syndicated from the U.S. Food and Drug Administration (FDA) drug enforcement reports database.