D-623-2013 Class II Terminated

Recalled by Baxter Healthcare Corp. — Deerfield, IL

FDA drug recall D-623-2013 was initiated by Baxter Healthcare Corp. on Feb 27, 2013 and is designated Class II. Reason for recall: Labeling Wrong Barcode; It may display wrong product code reflecting 0.9% Sodium Chloride Injection , USP 100 mL in MINI-BAG Plus container instead of 50 mL. The recall status is terminated (terminated May 11, 2015). Affected quantity: 317,280 bags.

Recall Details

Product Type
Drugs
Report Date
Jul 3, 2013
Initiation Date
Feb 27, 2013
Termination Date
May 11, 2015
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
317,280 bags

Product Description

0.9% Sodium Chloride Injection, USP, 50 mL Mini-Bag Plus Container, Rx only, distributed by Baxter Healthcare Corporation, Deerfield, IL 60015, USA, NDC 0338-0553-11

Reason for Recall

Labeling Wrong Barcode; It may display wrong product code reflecting 0.9% Sodium Chloride Injection , USP 100 mL in MINI-BAG Plus container instead of 50 mL.

Distribution Pattern

Nationwide and Singapore

Code Information

Lot: P293118; Exp Date: 10/13

Source

Dataset
openFDA drug recall enforcement reports
FDA record
This recall in openFDA (JSON)
Enforcement Report
Search FDA's Enforcement Report for D-623-2013
openFDA file date
Oct 27, 2026
Loaded by RegDataLab
Oct 29, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.