Medical device recalls Moderate risk

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

Recall date
May 23, 2025
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1361-2026
FDA classification
Class II
Brand / firm
Steris Corporation
Sold / distributed
US Nationwide distribution in the states of FL, NC, NY, OH, TN, TX, and VA.

Why it was recalled

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.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

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

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