# FDA recall D-1234-2014

> **Hospira, Inc.** · Class I · drug recall initiated 2013-09-16.

## Product

1% Lidocaine HCl Injection, USP, 10 mg/mL, NDC 0409-4276-01, Hospira, Inc., Lake Forest, IL 60045.

## Reason for recall

Presence of Particulate Matter: Oxidized stainless steel found in vial of 1% Lidocaine Hydrochloride Injection, USP.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-1234-2014
- **Recalling firm:** Hospira, Inc.
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2013-09-16
- **Report date:** 2014-04-23
- **Termination date:** 2014-11-04

- **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-1234-2014

## Citation

> AI Analytics. FDA recall D-1234-2014. Retrieved 2026-06-16 from https://api.ai-analytics.org/recall/D-1234-2014. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*