# FDA recall Z-0424-2023

> **Olympus Corporation of the Americas** · Class II · device recall initiated 2022-11-04.

## Product

HF Resection Electrodes, Model Numbers WA22602S, WA22603S, WA22621S and WA22657S

## Reason for recall

An incompatible HF cable may be packaged with the HF Resection Electrodes. This cable cannot be connected to the electrosurgical generator and may lead to delay or cancellation of the surgical procedure.

## Distribution

US Nationwide domestic distribution.

## Key facts

- **Recall number:** Z-0424-2023
- **Recalling firm:** Olympus Corporation of the Americas
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-11-04
- **Report date:** 2022-12-14

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Center Valley, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0424-2023

## Citation

> AI Analytics. FDA recall Z-0424-2023. Retrieved 2026-07-13 from https://api.ai-analytics.org/recall/Z-0424-2023. Source: US FDA. Licensed CC0.

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