# FDA recall D-0429-2015

> **Baxter Healthcare Corp** · Class II · drug recall initiated 2015-03-23.

## Product

0.9% Sodium Chloride Injection, USP, 50 mL, VIAFLEX Plastic Container Multi Pack, Rx Only, Baxter Healthcare Corporation, Deerfield, IL , Product code 2B1308, NDC 0338-0049-31

## Reason for recall

Lack of Assurance of Sterility; increased complaints received for leaks

## Distribution

Nationwide and Singapore

## Key facts

- **Recall number:** D-0429-2015
- **Recalling firm:** Baxter Healthcare Corp
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2015-03-23
- **Report date:** 2015-04-08
- **Termination date:** 2016-10-20

- **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-0429-2015

## Citation

> AI Analytics. FDA recall D-0429-2015. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/D-0429-2015. Source: US FDA. Licensed CC0.

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