# FDA recall Z-2162-2024

> **Beaver Visitec International, Inc.** · Class II · device recall initiated 2024-05-10.

## Product

Xstar Safety Slit Knife, 2.75 mm 45¿ Bevel Up, Model Number 378227, a component of CustomEye Kits, Numbers 584562, 5800109

## Reason for recall

The wrong configuration of the blade was in the package. The bevel was on the opposite side, instead of being in front (bevel up) it was in the back (bevel down).

## Distribution

Worldwide distribution - US Nationwide and the countries of Canada, UK, and Italy.

## Key facts

- **Recall number:** Z-2162-2024
- **Recalling firm:** Beaver Visitec International, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-05-10
- **Report date:** 2024-06-26

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Waltham, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2162-2024

## Citation

> AI Analytics. FDA recall Z-2162-2024. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-2162-2024. Source: US FDA. Licensed CC0.

---

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