# FDA recall D-0831-2016

> **Hospira Inc.** · Class II · drug recall initiated 2016-03-08.

## Product

Mannitol I.V., 20%, USP (20 g/ 100 mL), Packaged in 250 mL Bags, Rx Only, Hospira, Inc., Lake Forest, IL  60045,  NDC: 0409-7715-02, Barcode (01) 0 030409 771502 2

## Reason for recall

Chemical Contamination: Potential for contamination of the products with an aromatic hydrocarbon resin.

## Distribution

US: Nationwide and Singapore

## Key facts

- **Recall number:** D-0831-2016
- **Recalling firm:** Hospira Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2016-03-08
- **Report date:** 2016-04-27
- **Termination date:** 2017-12-06

- **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-0831-2016

## Citation

> AI Analytics. FDA recall D-0831-2016. Retrieved 2026-05-24 from https://api.ai-analytics.org/recall/D-0831-2016. Source: US FDA. Licensed CC0.

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