# FDA recall D-0490-2015

> **Hospira Inc.** · Class II · drug recall initiated 2015-04-07.

## Product

0.9% Sodium Chloride Injection, USP, 100 mL ADD-Vantage Unit, Rx only, Manufactured by Hospira Inc., Lake Forest, IL, 60045, NDC: 0409-7101-67

## Reason for recall

Lack of Sterility Assurance: The product has the potential to leak at the administrative port.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-0490-2015
- **Recalling firm:** Hospira Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2015-04-07
- **Report date:** 2015-04-29
- **Termination date:** 2016-11-04

- **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-0490-2015

## Citation

> AI Analytics. FDA recall D-0490-2015. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/D-0490-2015. Source: US FDA. Licensed CC0.

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