# FDA recall D-0324-2015

> **Hospira Inc.** · Class I · drug recall initiated 2014-09-11.

## Product

HEPARIN SODIUM, 1000 USP Heparin Units/500 mL (2 USP Heparin Units/mL), in 0.9% Sodium Chloride Injection, 500 mL flexible container unit, Rx only, Hospira Inc., Lake Forest, IL 60045, NDC 0409-7620-03

## Reason for recall

Presence of Particulate Matter: A particulate, confirmed as human hair, was found sealed between the tube and film at the round seal of the unused administrative port of the container.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-0324-2015
- **Recalling firm:** Hospira Inc.
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2014-09-11
- **Report date:** 2014-12-31
- **Termination date:** 2016-01-04

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Lake Forest, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0324-2015

## Citation

> AI Analytics. FDA recall D-0324-2015. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/D-0324-2015. Source: US FDA. Licensed CC0.

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