# FDA recall D-1159-2014

> **Baxter Healthcare Corp.** · Class I · drug recall initiated 2013-11-18.

## Product

Clinimix E 4.25/10 sulfite-free (4.25% Amino Acid with Electrolytes in 10% Dextrose with Calcium) Injection, 2000 mL CLARITY Dual Chamber Container bag, Rx only. Dist: Baxter Healthcare Corporation, One Baxter Parkway, Deerfield, IL 60015. NDC 0338-1115-04.

## Reason for recall

Presence of Particulate Matter: Particulate matter includes wood, sodium citrate and dextrose.

## Distribution

US Nationwide

## Key facts

- **Recall number:** D-1159-2014
- **Recalling firm:** Baxter Healthcare Corp.
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2013-11-18
- **Report date:** 2014-03-26
- **Termination date:** 2016-09-20

- **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-1159-2014

## Citation

> AI Analytics. FDA recall D-1159-2014. Retrieved 2026-06-16 from https://api.ai-analytics.org/recall/D-1159-2014. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
