# FDA recall D-0426-2015

> **Baxter Healthcare Corp.** · Class II · drug recall initiated 2015-03-18.

## Product

5% Dextrose Injection, USP, 1000mL in VIAFLEX Plastic Container, Rx only, Manufactured by Baxter Healthcare Corp., North Cove, North Carolina Facility Highway 221 North, Marion, NC 28752 for Baxter Healthcare Corporation, One Baxter Parkway, Deerfield, IL 60015. NDC 0338-0017-04

## Reason for recall

Lack of Assurance of Sterility. Complaints were receive of missing closures and/or leaks which may compromise product sterility.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-0426-2015
- **Recalling firm:** Baxter Healthcare Corp.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2015-03-18
- **Report date:** 2015-04-01
- **Termination date:** 2016-02-24

- **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-0426-2015

## Citation

> AI Analytics. FDA recall D-0426-2015. Retrieved 2026-06-08 from https://api.ai-analytics.org/recall/D-0426-2015. Source: US FDA. Licensed CC0.

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