# FDA recall Z-0874-2026

> **Aizu Olympus Co., Ltd.** · Class II · device recall initiated 2025-10-31.

## Product

Olympus OER-Mini

## Reason for recall

Inform existing affected device customers about pertinent Warnings/Cautions, existing recommended maintenance  schedules and that only properly trained personnel conduct repairs and maintenance.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-0874-2026
- **Recalling firm:** Aizu Olympus Co., Ltd.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-10-31
- **Report date:** 2025-12-10

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Aizuwakamatsu, Japan

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0874-2026

## Citation

> AI Analytics. FDA recall Z-0874-2026. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-0874-2026. Source: US FDA. Licensed CC0.

---

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