# FDA recall D-1096-2014

> **Hospira Inc.** · Class II · drug recall initiated 2014-02-11.

## Product

0.9% Sodium Chloride Injection, USP 1000 mL Flexible Container, Rx Only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7983-09

## Reason for recall

Lack of Assurance of Sterility:Solution leaking through the port cover of the primary container, which was identified during a retain sample visual inspection.

## Distribution

Nationwide and Puerto Rico

## Key facts

- **Recall number:** D-1096-2014
- **Recalling firm:** Hospira Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2014-02-11
- **Report date:** 2014-03-12
- **Termination date:** 2015-03-17

- **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-1096-2014

## Citation

> AI Analytics. FDA recall D-1096-2014. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/D-1096-2014. Source: US FDA. Licensed CC0.

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