# FDA recall Z-1908-2026

> **Olympus Corporation of the Americas** · Class II · device recall initiated 2026-03-25.

## Product

OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2138.

## Reason for recall

Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.

## Distribution

Worldwide distribution - US Nationwide and the countries of Canada, China, Hong Kong, Japan, South Korea and Taiwan.

## Key facts

- **Recall number:** Z-1908-2026
- **Recalling firm:** Olympus Corporation of the Americas
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-03-25
- **Report date:** 2026-04-29

- **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-1908-2026

## Citation

> AI Analytics. FDA recall Z-1908-2026. Retrieved 2026-05-24 from https://api.ai-analytics.org/recall/Z-1908-2026. Source: US FDA. Licensed CC0.

---

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