# FDA recall D-0392-2015

> **Hospira Inc.** · Class I · drug recall initiated 2014-07-10.

## Product

LACTATED RINGER'S and 5% DEXTROSE Injection USP, 1000 mL, flexible containers, Rx Only, Hospira, Inc., Lake Forest, IL 600045,  NDC 0409-7929-09

## Reason for recall

Non-Sterility: Confirmed customer complaint of particulate matter floating within the solution of the primary container, consistent with mold.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-0392-2015
- **Recalling firm:** Hospira Inc.
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2014-07-10
- **Report date:** 2015-02-25
- **Termination date:** 2015-11-23

- **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-0392-2015

## Citation

> AI Analytics. FDA recall D-0392-2015. Retrieved 2026-05-28 from https://api.ai-analytics.org/recall/D-0392-2015. Source: US FDA. Licensed CC0.

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