Class II

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

Steris Corporation · May 23, 2025

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.

States Affected

NATIONWIDE

Quantity Affected

10 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1361-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Steris Corporation Medical Device Recall: Barco MNA with the HexaVue IP Integration System, Model/Catalog Number: MNA-6x0-H | SafeCheck