# FDA recall D-1583-2014

> **Baxter Healthcare Corp.** · Class II · drug recall initiated 2014-07-30.

## Product

0.9% Sodium Chloride Injection, USP, 500 mL, VIAFLEX Plastic Container, Baxter Healthcare Corporation, Deerfield, IL NDC 0338-0049-03

## Reason for recall

Lack of Assurance of Sterility; complaints of mold in the overpouch

## Distribution

Nationwide

## Key facts

- **Recall number:** D-1583-2014
- **Recalling firm:** Baxter Healthcare Corp.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2014-07-30
- **Report date:** 2014-09-17
- **Termination date:** 2016-06-08

- **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-1583-2014

## Citation

> AI Analytics. FDA recall D-1583-2014. Retrieved 2026-05-27 from https://api.ai-analytics.org/recall/D-1583-2014. Source: US FDA. Licensed CC0.

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