# FDA recall D-215-2013

> **Hospira, Inc.** · Class III · drug recall initiated 2012-06-21.

## Product

Lactated Ringer's Injection, USP, 1000 mL, Rx only, Manufactured by Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7953-09

## Reason for recall

CGMP Deviations: Shipment of product not approved for release.

## Distribution

NC

## Key facts

- **Recall number:** D-215-2013
- **Recalling firm:** Hospira, Inc.
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2012-06-21
- **Report date:** 2013-04-03
- **Termination date:** 2013-03-28

- **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-215-2013

## Citation

> AI Analytics. FDA recall D-215-2013. Retrieved 2026-05-27 from https://api.ai-analytics.org/recall/D-215-2013. Source: US FDA. Licensed CC0.

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