# FDA recall Z-1375-2026

> **Olympus Corporation of the Americas** · Class II · device recall initiated 2025-10-22.

## Product

Olympus Thunderbeat 5 mm, 35 cm, Front-Actuated Grip

## Reason for recall

Firm is initiating a removal due to continued reports of adverse events.

## Distribution

Worldwide distribution - US Nationwide and the countries of Brazil, Canada, Germany, Mexico, and Japan.

## Key facts

- **Recall number:** Z-1375-2026
- **Recalling firm:** Olympus Corporation of the Americas
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-10-22
- **Report date:** 2026-02-25

- **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-1375-2026

## Citation

> AI Analytics. FDA recall Z-1375-2026. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1375-2026. Source: US FDA. Licensed CC0.

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