# FDA recall D-313-2013

> **Hospira Inc.** · Class II · drug recall initiated 2013-02-26.

## Product

Diazepam Injection, USP 5 mg/mL, 10 mL, Multiple-dose fliptop vial, RX only, HOSPIRA, INC. LAKE FOREST, IL 60045 USA, NDC 0409-3213-12

## Reason for recall

Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.

## Distribution

Nationwide and Puerto Rico

## Key facts

- **Recall number:** D-313-2013
- **Recalling firm:** Hospira Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2013-02-26
- **Report date:** 2013-05-15
- **Termination date:** 2014-11-10

- **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-313-2013

## Citation

> AI Analytics. FDA recall D-313-2013. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-313-2013. Source: US FDA. Licensed CC0.

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