# FDA recall Z-0601-2026

> **Stryker Corporation** · Class II · device recall initiated 2025-10-31.

## Product

NICO BrainPath;  Product Number/Product Name    NN-8024  BrainPath Shephard's Hook - Greenberg;  NN-8025  BrainPath Shephard's Hook - Sugita;  NN-8026  BrainPath Shephard's Hook - Budde;  NN-8042  BrainPath Shephard's Hook - Greenberg LK;

## Reason for recall

Tape used to secure components within packaging contains latex, despite products being labeled as latex-free. Latex could potentially cause an allergic reaction.

## Distribution

Worldwide distribution - US Nationwide and the countries of Australia, Belgium, Canada, England, Ireland, Italy, Kuwait, Singapore, Slovenia, Spain, and the Netherlands.

## Key facts

- **Recall number:** Z-0601-2026
- **Recalling firm:** Stryker Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-10-31
- **Report date:** 2025-12-03

- **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-0601-2026

## Citation

> AI Analytics. FDA recall Z-0601-2026. Retrieved 2026-07-16 from https://api.ai-analytics.org/recall/Z-0601-2026. Source: US FDA. Licensed CC0.

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