# FDA recall Z-2261-2024

> **Stryker Corporation** · Class II · device recall initiated 2024-06-03.

## Product

This product is a single use sterile device that is used to direct the lesion to the targeted site. Each cannula contains a stylet that is removed once the cannula is placed. The electrode is then inserted into the cannula. Catalog Number: 0406-630-225

## Reason for recall

Expired Products distributed to customers

## Distribution

US Nationwide distribution in the states of Arkansas, California, Colorado, Florida, Michigan.

## Key facts

- **Recall number:** Z-2261-2024
- **Recalling firm:** Stryker Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-06-03
- **Report date:** 2024-07-10

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Portage, MI, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2261-2024

## Citation

> AI Analytics. FDA recall Z-2261-2024. Retrieved 2026-07-31 from https://api.ai-analytics.org/recall/Z-2261-2024. Source: US FDA. Licensed CC0.

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