# FDA recall Z-0982-2025

> **Stryker Corporation** · Class II · device recall initiated 2023-06-28.

## Product

stryker 3.0MM Precision Neuro Match Head, REF 5820-107-530, used to cut bone and bone cement during neurosurgery

## Reason for recall

There is potential the device inside the package may not match the product information on the outer label (e.g., label states 5820-107-430 but package contains a 5820-107-530 device or vice versa).

## Distribution

Worldwide distribution - US Nationwide and the countries of UK, Netherlands, New Zealand.

## Key facts

- **Recall number:** Z-0982-2025
- **Recalling firm:** Stryker Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-06-28
- **Report date:** 2025-01-29

- **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-0982-2025

## Citation

> AI Analytics. FDA recall Z-0982-2025. Retrieved 2026-07-16 from https://api.ai-analytics.org/recall/Z-0982-2025. Source: US FDA. Licensed CC0.

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