# FDA recall D-1326-2015

> **Baxter Healthcare Corp.** · Class II · drug recall initiated 2015-07-02.

## Product

0.9% Sodium Chloride Injection USP, 500 mL in VIAFLEX Plastic Container, Baxter Healthcare Corporation Deerfield, IL 60015,   NDC 0338-0049-03.

## Reason for recall

Presence of Particulate Matter and Lack of Assurance of Sterility: The firm received a complaint for customer of presence of particulate matter, leaky containers, and missing port protectors.

## Distribution

TX and TN

## Key facts

- **Recall number:** D-1326-2015
- **Recalling firm:** Baxter Healthcare Corp.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2015-07-02
- **Report date:** 2015-08-19
- **Termination date:** 2016-05-26

- **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-1326-2015

## Citation

> AI Analytics. FDA recall D-1326-2015. Retrieved 2026-05-28 from https://api.ai-analytics.org/recall/D-1326-2015. Source: US FDA. Licensed CC0.

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