# FDA recall Z-2415-2024

> **Olympus Corporation of the Americas** · Class II · device recall initiated 2024-06-21.

## Product

ESG-410 Electrosurgical Generator- In conjunction with electrosurgical accessories intended for cutting and coagulation of tissue in open, laparoscopic , and endoscopic surgeries  Model/Catalog Number: WA91307C

## Reason for recall

Electrosurgical Generators ESG-410 does not power on upon use, may result in delays in initiating treatment or prolonged surgery

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-2415-2024
- **Recalling firm:** Olympus Corporation of the Americas
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-06-21
- **Report date:** 2024-07-31

- **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-2415-2024

## Citation

> AI Analytics. FDA recall Z-2415-2024. Retrieved 2026-07-11 from https://api.ai-analytics.org/recall/Z-2415-2024. Source: US FDA. Licensed CC0.

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