# FDA recall D-012-2014

> **Hospira Inc.** · Class II · drug recall initiated 2013-09-24.

## Product

Metoclopramide Injection, USP 10 mg (5mg/mL), 2 mL Single-dose Vial, Rx Only, Sterile, Hospira Inc., Lake Forest, IL, 60045, USA, NDC 0409-3414-01

## Reason for recall

Presence of Particulate Matter: Potential vendor glass issue - glass spiticules (glass strands) were identified during site inspection of the vials.

## Distribution

Nationwide and Puerto Rico

## Key facts

- **Recall number:** D-012-2014
- **Recalling firm:** Hospira Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2013-09-24
- **Report date:** 2013-11-27
- **Termination date:** 2014-10-06

- **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-012-2014

## Citation

> AI Analytics. FDA recall D-012-2014. Retrieved 2026-05-24 from https://api.ai-analytics.org/recall/D-012-2014. Source: US FDA. Licensed CC0.

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