# FDA recall D-262-2013

> **Hospira Inc.** · Class I · drug recall initiated 2013-01-25.

## Product

Lactated Ringer's and 5% Dextrose Injection, USP, 1000 mL flexible container, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA; NDC 0409-7929-09.

## Reason for recall

Non-Sterility: Confirmed customer complaint of product contaminated with mold.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-262-2013
- **Recalling firm:** Hospira Inc.
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2013-01-25
- **Report date:** 2013-04-24
- **Termination date:** 2015-08-21

- **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-262-2013

## Citation

> AI Analytics. FDA recall D-262-2013. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-262-2013. Source: US FDA. Licensed CC0.

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