# FDA recall D-623-2013

> **Baxter Healthcare Corp.** · Class II · drug recall initiated 2013-02-27.

## Product

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

Nationwide and Singapore

## Key facts

- **Recall number:** D-623-2013
- **Recalling firm:** Baxter Healthcare Corp.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2013-02-27
- **Report date:** 2013-07-03
- **Termination date:** 2015-05-11

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Deerfield, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-623-2013

## Citation

> AI Analytics. FDA recall D-623-2013. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-623-2013. Source: US FDA. Licensed CC0.

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