# FDA recall D-0726-2026

> **Fresenius Kabi USA, LLC** · Class II · drug recall initiated 2026-07-16.

## Product

Lidocaine HCl Injection, USP, 2%, 100 mg per 5 mL (20 mg per mL), 25 Single Dose Vials, 5 mL per vial,  Rx only, Sterile, Fresenius Kabi, Lake Zurich, IL 60047 NDC Tray: 63323-208-05; NDC Vial:  63323-208-01

## Reason for recall

Presence of Particulate Matter: Hair was found in products

## Distribution

Nationwide within in the USA

## Key facts

- **Recall number:** D-0726-2026
- **Recalling firm:** Fresenius Kabi USA, LLC
- **Classification:** Class II
- **Product type:** drug
- **Status:** Ongoing
- **Initiation date:** 2026-07-16
- **Report date:** 2026-07-29

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Lake Zurich, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0726-2026

## Citation

> AI Analytics. FDA recall D-0726-2026. Retrieved 2026-09-02 from https://api.ai-analytics.org/recall/D-0726-2026. Source: US FDA. Licensed CC0.

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