# FDA recall Z-0689-2024

> **Shirakawa Olympus Co., Ltd.** · Class II · device recall initiated 2023-12-04.

## Product

Model No. CYF-VH, CYSTO-NEPHRO VIDEOSCOPE

## Reason for recall

Olympus has updated the instructions for use: Reusable cleaning brushes have been removed from the manual cleaning. Single use brushes remain compatible.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-0689-2024
- **Recalling firm:** Shirakawa Olympus Co., Ltd.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-12-04
- **Report date:** 2024-01-17

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Nishishirakawa-Gun, Japan

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0689-2024

## Citation

> AI Analytics. FDA recall Z-0689-2024. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-0689-2024. Source: US FDA. Licensed CC0.

---

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