# FDA recall D-0276-2015

> **Baxter Healthcare Corp.** · Class II · drug recall initiated 2014-10-30.

## Product

Heparin Sodium in 0.9% Sodium Chloride Injection, 1000 USP Heparin Units, 500 mL in a VIAFLEX Plus Container, Rx only, Manufactured for Baxter Healthcare Corporation, One Baxter Parkway, Deerfield, IL 60015 by Baxter Healthcare Corporation 250 Road 144 Jayuya, Puerto Rico, 00664, NDC 0338-0431-03

## Reason for recall

Subpotent Drug: Heparin raw material was found to have low potency

## Distribution

Nationwide

## Key facts

- **Recall number:** D-0276-2015
- **Recalling firm:** Baxter Healthcare Corp.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2014-10-30
- **Report date:** 2014-12-03
- **Termination date:** 2016-09-22

- **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-0276-2015

## Citation

> AI Analytics. FDA recall D-0276-2015. Retrieved 2026-05-28 from https://api.ai-analytics.org/recall/D-0276-2015. Source: US FDA. Licensed CC0.

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