# FDA recall D-1591-2014

> **Baxter Healthcare Corp.** · Class I · drug recall initiated 2014-07-11.

## Product

0.9% Sodium Chloride Injection USP, packaged in a) 50 mL VIAFLEX Container bags, NDC 0338-0049-41, Product Code 2B1306; and b) 100 mL VIAFLEX Container bags, NDC 0338-0049-18, Product Code 2B1302, Rx only, Baxter Healthcare Corporation, Deerfield, IL  60015 USA.

## Reason for recall

Presence of Particulate Matter: particulate matter identified as fibers and/or plastics.

## Distribution

Nationwide, Puerto Rico, Singapore, and Hong Kong

## Key facts

- **Recall number:** D-1591-2014
- **Recalling firm:** Baxter Healthcare Corp.
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2014-07-11
- **Report date:** 2014-09-24
- **Termination date:** 2016-09-21

- **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-1591-2014

## Citation

> AI Analytics. FDA recall D-1591-2014. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/D-1591-2014. Source: US FDA. Licensed CC0.

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