D-623-2013 Class II Terminated
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