# FDA recall D-0284-2015

> **Hospira Inc.** · Class II · drug recall initiated 2014-10-14.

## Product

Normosol-R Multiple Electrolytes Injection Type 1, USP, 1000 mL container,  Rx Only, Manufactured by Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7967-09.

## Reason for recall

Lack of Assurance of Sterility: Potential of punctures through the overwrap and primary container which may result in IV bag leaks.

## Distribution

Nationwide, Puerto Rico, and U.S. Virgin Islands.

## Key facts

- **Recall number:** D-0284-2015
- **Recalling firm:** Hospira Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2014-10-14
- **Report date:** 2014-12-03
- **Termination date:** 2015-12-28

- **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-0284-2015

## Citation

> AI Analytics. FDA recall D-0284-2015. Retrieved 2026-05-28 from https://api.ai-analytics.org/recall/D-0284-2015. Source: US FDA. Licensed CC0.

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