# FDA recall D-1542-2014

> **Baxter Healthcare Corp** · Class II · drug recall initiated 2014-08-04.

## Product

ProSol - sulfite-free (Amino Acid) Injection, 20%, 2000 mL VIAFLEX container bag, Rx only, Baxter Healthcare Corporation, Clinitec Nutrition Division, Deerfield, IL  60015 USA, Product Code 2B6186, NDC 0338-0499-06.

## Reason for recall

Presence of Particulate Matter: identification of particulates in a retention sample that have been identified as a mixture of the amino acid leucine and inorganic material (containing iron, silicone and chlorine).

## Distribution

Nationwide

## Key facts

- **Recall number:** D-1542-2014
- **Recalling firm:** Baxter Healthcare Corp
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2014-08-04
- **Report date:** 2014-08-27
- **Termination date:** 2015-06-10

- **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-1542-2014

## Citation

> AI Analytics. FDA recall D-1542-2014. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/D-1542-2014. Source: US FDA. Licensed CC0.

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