# FDA recall D-1433-201

> **Hospira Inc.** · Class II · drug recall initiated 2014-06-27.

## Product

Fentanyl Citrate Injection, USP, 2500 mcg Fentanyl/50 mL, C-II, (50 mcg/mL), 50 mL Single-dose Fliptop Vial, Rx only.  Hospira, Inc., Lake Forest, IL 60045. NDC: 0409-9094-61.

## Reason for recall

Lack of Assurance of Sterility: Fliptop vial crimps are loose or missing.

## Distribution

U.S. Nationwide

## Key facts

- **Recall number:** D-1433-201
- **Recalling firm:** Hospira Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2014-06-27
- **Report date:** 2014-07-23
- **Termination date:** 2015-09-09

- **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-1433-201

## Citation

> AI Analytics. FDA recall D-1433-201. Retrieved 2026-05-27 from https://api.ai-analytics.org/recall/D-1433-201. Source: US FDA. Licensed CC0.

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