RecallRadar

FDA Device recall Z-1361-2026

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

On 2026-02-18 the FDA classified a Class II recall of Barco MNA with the HexaVue IP Integration System, Model/Catalog Number: MNA-6x0-H by Steris, citing 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 configur….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1361-2026
ClassificationClass II
Statusongoing
Initiated2025-05-23
Published2026-02-18
Last updated2026-09-13 11:58 UTC
CompanySteris
DistributionUS

Product

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

Reason

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.

Identifiers

code_info
UDI-DI: 00724995220570; Serial Numbers for MNAs: 2531542441, 2531542470, 2531543549, 2531543611, 2531572419, 2531572433…UDI-DI: 00724995220570; Serial Numbers for MNAs: 2531542441, 2531542470, 2531543549, 2531543611, 2531572419, 2531572433, 2531572440, 2531588558, 2531593768, and 2531595829

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1361-2026%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.