# FDA recall D-0254-2015

> **Hospira Inc.** · Class III · drug recall initiated 2014-11-07.

## Product

Sterile powder Vancomycin Hydrochloride for Injection, USP, Equivalent to 1 g in 25 ml fliptop vial, 10-count tray, Rx only, Manufactured by Hospira, Inc. Lake Forest, IL 60045,  NDC 0409-6533-01.

## Reason for recall

Correct Labeled Product Mispack: Product tray containing vials was mislabeled to contain another product.

## Distribution

Nationwide.

## Key facts

- **Recall number:** D-0254-2015
- **Recalling firm:** Hospira Inc.
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2014-11-07
- **Report date:** 2014-11-26
- **Termination date:** 2017-03-22

- **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-0254-2015

## Citation

> AI Analytics. FDA recall D-0254-2015. Retrieved 2026-05-28 from https://api.ai-analytics.org/recall/D-0254-2015. Source: US FDA. Licensed CC0.

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