# FDA recall D-1278-2014

> **Hospira Inc.** · Class I · drug recall initiated 2013-12-23.

## Product

Lidocaine HCl  Injection, USP, 2%, 20 mg per mL, packaged in 5-mL single-dose vials, 10 vials per box, Rx Only,  Hospira, Inc., Lake Forest, IL. 60045, NDC 0409-2066-05.

## Reason for recall

Presence of Particulate Matter- Confimed customer complaint of  particulates embedded in glass container and in contact with product solution.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-1278-2014
- **Recalling firm:** Hospira Inc.
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2013-12-23
- **Report date:** 2014-05-07
- **Termination date:** 2014-10-07

- **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-1278-2014

## Citation

> AI Analytics. FDA recall D-1278-2014. Retrieved 2026-07-02 from https://api.ai-analytics.org/recall/D-1278-2014. Source: US FDA. Licensed CC0.

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