# FDA recall D-1131-2015

> **Baxter Healthcare Corp** · Class II · drug recall initiated 2015-06-03.

## Product

Heparin Sodium and 0.9% Sodium Chloride Injection, 1000 USP Heparin Units, 500 mL in a VIAFLEX Plus Container, Rx Only, Baxter Healthcare Corporation, Deerfield, IL --- NDC 0338-0431-03

## Reason for recall

Subpotent Drug; out of specification results for heparin raw material

## Distribution

Nationwide

## Key facts

- **Recall number:** D-1131-2015
- **Recalling firm:** Baxter Healthcare Corp
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2015-06-03
- **Report date:** 2015-06-17
- **Termination date:** 2017-03-14

- **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-1131-2015

## Citation

> AI Analytics. FDA recall D-1131-2015. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/D-1131-2015. Source: US FDA. Licensed CC0.

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