# FDA recall D-1815-2015

> **Hospira, Inc.** · Class II · drug recall initiated 2015-08-25.

## Product

1% Lidocaine HCl Injection, USP, 10 mg/mL, 30 mL Vial, Single-dose Preservative Free, Rx only, Hospira, Inc., Lake Forest, IL 60045, USA, NDC 0409-4279-02

## Reason for recall

Presence of Particulate Matter: particulate matter identified as iron oxide, was found embedded in the neck of glass vials.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-1815-2015
- **Recalling firm:** Hospira, Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Ongoing
- **Initiation date:** 2015-08-25
- **Report date:** 2015-09-30

- **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-1815-2015

## Citation

> AI Analytics. FDA recall D-1815-2015. Retrieved 2026-05-27 from https://api.ai-analytics.org/recall/D-1815-2015. Source: US FDA. Licensed CC0.

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