# FDA recall D-0957-2016

> **Baxter Healthcare Corp.** · Class I · drug recall initiated 2015-12-15.

## Product

0.9% Sodium Chloride Injection, USP, 250 mL VIAFLEX Plastic Container Bag, Rx Only, Manufactured by Baxter Healthcare Corporation, Deerfield, IL 60015, NDC 0338-0049-02

## Reason for recall

Presence of Particulate Matter: Confirmed customer compliants of finding an insect floating in the primary container of each product.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-0957-2016
- **Recalling firm:** Baxter Healthcare Corp.
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2015-12-15
- **Report date:** 2016-06-15
- **Termination date:** 2022-04-15

- **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-0957-2016

## Citation

> AI Analytics. FDA recall D-0957-2016. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/D-0957-2016. Source: US FDA. Licensed CC0.

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