# FDA recall D-1550-2014

> **Baxter Healthcare Corp.** · Class I · drug recall initiated 2014-05-12.

## Product

0.9 % Sodium Chloride Injection, USP, 1000 mL in VIAFLEX Plastic Container, Baxter Healthcare Corporation, Deerfield, IL 60015

## Reason for recall

Presence of Particulate Matter; blue polyisoprene shavings found inside the bag port tubes

## Distribution

Nationwide

## Key facts

- **Recall number:** D-1550-2014
- **Recalling firm:** Baxter Healthcare Corp.
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2014-05-12
- **Report date:** 2014-08-27
- **Termination date:** 2015-06-29

- **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-1550-2014

## Citation

> AI Analytics. FDA recall D-1550-2014. Retrieved 2026-05-27 from https://api.ai-analytics.org/recall/D-1550-2014. Source: US FDA. Licensed CC0.

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