Reported Jul 2, 2025 · Ongoing

Model: Description/REF: MNA-420: MNA-420 ENC -H/K9303320, MNA-420 DEC -H V2/K9303331; MNA-440: MNA-440 ENC -H/K9303300,…

Barco N.V.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Barco N.V. · President Kennedypark 35 · Kortrijk · N/A

Is this the product you have?

5 of 5 products

Products covered by this recall
#Product as published
1Model: Description/REF: MNA-420: MNA-420 ENC -H/K9303320, MNA-420 DEC -H V2/K9303331
2MNA-440: MNA-440 ENC -H/K9303300, MNA-440 DEC -H V2/K9303311
3MNA-620: MNA-620 DEC -H/K9306210, MNA-620 ENC -H/K9306220
4and MNA-640: MNA-640 DEC -H/K9306410, MNA-640 ENC -H/K9306420
5components of the NexxisOR system
Lot codes and dates
  • REF/UDI-DI/Serial Number

    221 of 221 codes

    • K9303320/05415334002364/2531531598
    • 2531531604
    • 2531534397
    • 2531534420
    • 2531534430
    • 2531534466
    • 2531534905
    • 2531534948
    • 2531534956
    • 2531536564
    • 2531554560
    • 2531572616
    • 2531572628
    • 2531572634
    • 2531591962
    • 2531591973
    • 2531591992
    • 2531592064
    • 2531592096
    • 2531593814
    • 2531593818
    • 2531593823
    • 2531597597
    • 2531610546
    • 2531610547
    • 2531610572
    • 2531610578
    • 2531610580
    • 2531612404
    • 2531612420
    • 2531612424
    • 2531612430
    • 2531612431
    • 2531612432
    • 2531612433
    • 2531612434
    • 2531612436
    • 2531612442
    • 2531623109
    • 2531623114
    • 2531623131
    • 2531623133
    • 2531623141
    • 2531635578
    • 2531635582
    • 2531639224
    • 2531639261
    • 2531639263
    • 2531639353
    • 2531640594
    • 2531640597
    • 2531640598
    • 2531640603
    • 2531640626
    • 2531640634
    • 2531540640
    • 2531640646
    • 2531640658
    • 2531640660
    • K9303331/05415334026827/2531533275
Amount recalled
221

Where it was sold

Why it was recalled

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

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 7:36 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.