# FDA recall D-66637-001

> **Hospira Inc.** · Class II · drug recall initiated 2013-10-11.

## Product

Propofol Injectable Emulsion, 1%, 200 mg/20 mL (10 mg/mL), 20 mL single patient infusion vial packaged in 5 Units x 20 mL per carton, Rx Only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-4699-30.

## Reason for recall

Presence of Particulate Matter: Visible particles embedded in the glass identified during a retain sample inspection.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-66637-001
- **Recalling firm:** Hospira Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2013-10-11
- **Report date:** 2013-11-13
- **Termination date:** 2014-10-28

- **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-66637-001

## Citation

> AI Analytics. FDA recall D-66637-001. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/D-66637-001. Source: US FDA. Licensed CC0.

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