# FDA recall Z-1488-2026

> **Olympus Corporation of the Americas** · Class II · device recall initiated 2026-01-29.

## Product

Olympus Single use Biopsy Valve. Model/Catalog Number: MAJ-210. 20 units per box.    The MAJ-210 has been designed to be attached to the instrument channel port of compatible endoscopes to prevent reflux of body fluids.

## Reason for recall

Potential for rubber fragment detachment during use.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-1488-2026
- **Recalling firm:** Olympus Corporation of the Americas
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-01-29
- **Report date:** 2026-03-11

- **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-1488-2026

## Citation

> AI Analytics. FDA recall Z-1488-2026. Retrieved 2026-09-04 from https://api.ai-analytics.org/recall/Z-1488-2026. Source: US FDA. Licensed CC0.

---

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