Barco N.V.: Device Recall

Recall #Z-1994-2025 · 05/09/2025

Class II: Risk

Recall Details

Recall Number
Z-1994-2025
Classification
Class II
Product Type
Device
Recalling Firm
Barco N.V.
Status
Ongoing
Date Initiated
05/09/2025
Location
Kortrijk, Belgium
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
221

Reason for Recall

Cathode ray tube display system encoders and decoders have same MAC address; new system setup with two or more affected units can lead to systems not functioning reliably:audio, video and/or control signals might be interrupted or fall away, displays might switch to failover and back multiple times, devices/sources/sinks might not be discovered/available, might lead to delayed/prolonged procedures

Product Description

Model: Description/REF: MNA-420: MNA-420 ENC -H/K9303320, MNA-420 DEC -H V2/K9303331; MNA-440: MNA-440 ENC -H/K9303300, MNA-440 DEC -H V2/K9303311; MNA-620: MNA-620 DEC -H/K9306210, MNA-620 ENC -H/K9306220; and MNA-640: MNA-640 DEC -H/K9306410, MNA-640 ENC -H/K9306420; components of the NexxisOR system

Distribution Pattern

US Nationwide distribution in the states of TX, OH.

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.