# FDA recall D-169-2013

> **Hospira, Inc.** · Class II · drug recall initiated 2013-01-10.

## Product

Furosemide Injection USP (10 mg/mL), 4 mL in 5 mL Fliptop Vial, Rx only, Hospira Inc., Lake Forest, IL --- NDC 0409-6102-04

## Reason for recall

Lack of Assurance of Sterility; possible loose crimp applied to fliptop vial

## Distribution

Nationwide

## Key facts

- **Recall number:** D-169-2013
- **Recalling firm:** Hospira, Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2013-01-10
- **Report date:** 2013-03-06
- **Termination date:** 2014-10-08

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Rocky Mount, NC, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-169-2013

## Citation

> AI Analytics. FDA recall D-169-2013. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/D-169-2013. Source: US FDA. Licensed CC0.

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