# FDA recall D-608-2013

> **Hospira Inc.** · Class II · drug recall initiated 2013-06-06.

## Product

0.9% Sodium Chloride Injection, USP, 250 mL single dose Flexible Plastic Container, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-7983-02

## Reason for recall

Lack of Assurance of Sterility: The product has the potential for solution to leak at or near the administrative port of the primary container.

## Distribution

Nationwide and Puerto Rico

## Key facts

- **Recall number:** D-608-2013
- **Recalling firm:** Hospira Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2013-06-06
- **Report date:** 2013-06-26
- **Termination date:** 2015-05-15

- **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-608-2013

## Citation

> AI Analytics. FDA recall D-608-2013. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/D-608-2013. Source: US FDA. Licensed CC0.

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