# FDA recall Z-1361-2026

> **Steris Corporation** · Class II · device recall initiated 2025-05-23.

## Product

Barco MNA with the HexaVue IP Integration System, Model/Catalog Number: MNA-6x0-H

## Reason for recall

This is a sub-recall of event RES 96885. The supplier identified that during their manufacturing process for a limited batch of MNA-6x0 (adapter) components the incorrect configuration file was used.

## Distribution

US Nationwide distribution in the states of FL, NC, NY, OH, TN, TX, and VA.

## Key facts

- **Recall number:** Z-1361-2026
- **Recalling firm:** Steris Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-05-23
- **Report date:** 2026-02-18

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Mentor, OH, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1361-2026

## Citation

> AI Analytics. FDA recall Z-1361-2026. Retrieved 2026-08-18 from https://api.ai-analytics.org/recall/Z-1361-2026. Source: US FDA. Licensed CC0.

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