# FDA recall Z-2339-2025

> **Olympus Corporation of the Americas** · Class II · device recall initiated 2025-07-25.

## Product

Electrosurgical, Cutting and Coagulation and Accessories. Electrosurgical Generator ESG-410. Model Number: WA91307C.     The ESG-410 Electrosurgical Generator is an electrosurgical generator which utilizes monopolar and bipolar high frequency current and supports ultrasonic instruments during open surgery, laparoscopic surgery, including single-site surgery, and endoscopic surgery.

## Reason for recall

Potential for the ESG-410 Electrosurgical Generator to display an error message: "E0662 System Error", followed by either automatic single reboots of the device, or continuous reboot 'loops'.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-2339-2025
- **Recalling firm:** Olympus Corporation of the Americas
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-07-25
- **Report date:** 2025-08-27

- **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-2339-2025

## Citation

> AI Analytics. FDA recall Z-2339-2025. Retrieved 2026-08-12 from https://api.ai-analytics.org/recall/Z-2339-2025. Source: US FDA. Licensed CC0.

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