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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device
Medical Devices/Surgical Equipment

Barco NexxisOR System Components Recalled for Display and Signal Failures

Agency Publication Date: June 20, 2025
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Summary

Barco N.V. is recalling 221 NexxisOR system components, including specific MNA-420, MNA-440, MNA-620, and MNA-640 encoder and decoder models. These devices, which are used to manage audio and video signals in operating rooms, may have duplicate network identification addresses (MAC addresses). If two or more affected units are used in the same system, it can cause the display to flicker, signals to drop out entirely, or the system to fail to recognize connected medical devices. No injuries have been reported, but these failures can lead to significant delays or prolonged surgical procedures.

Risk

The duplicate addresses cause network conflicts that interrupt critical audio, video, and control signals during medical procedures. This reliability failure may result in surgeons losing their primary display view or being unable to access connected video sources, potentially extending the time a patient is under anesthesia or delaying life-saving interventions.

What You Should Do

  1. This recall involves NexxisOR system components, specifically the MNA-420, MNA-440, MNA-620, and MNA-640 encoder and decoder models manufactured by Barco N.V.
  2. Identify affected units by checking the model and serial numbers located on the device labels. See the Affected Products section below for the full list of affected codes.
  3. Stop using the recalled device and disconnect it from your surgical network if you have identified a duplicate address conflict.
  4. Contact Barco N.V. or your authorized medical device distributor to arrange for a return, replacement, or on-site correction of the affected hardware.
  5. Call the FDA's medical device recall hotline at 1-888-463-6332 (1-888-INFO-FDA) for additional assistance or to report any performance issues.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: NexxisOR MNA-420 ENC -H
Model / REF:
K9303320
Serial Numbers (59):
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
UDI:
05415334002364
Product: NexxisOR MNA-420 DEC -H V2
Model / REF:
K9303331
Serial Numbers:
2531533275
2531533289
2531533292
2531533293
2531533304
2531533310
2531533312
2531533314
2531533316
2531533353
2531533356
2531534284
2531534292
2531534362
2531537718
2531540799
2531569738
2531582287
2531582290
2531582311
2531582315
2531582378
2531582750
2531582755
2531582790
2531582791
2531582826
2531582827
2531582829
2531584018
2531584044
2531537696
2531537726
UDI:
05415334026827
Product: NexxisOR MNA-440 ENC -H
Model / REF:
K9303300
Serial Numbers:
2531537815
2531557845
2531557866
2531558588
2531558727
2531558738
2531558753
2531558754
2531558759
2531561761
2531561785
2531572541
2531572557
2531572568
2531572576
2531572847
2531572862
2531572872
2531633606
2531633662
UDI:
05415334002180
Product: NexxisOR MNA-440 DEC -H V2
Model / REF:
K9303311
Serial Numbers:
2531537674
2531572141
2531580810
2531580935
2531582319
2531582331
2531582341
2531588386
2531588401
2531588404
2531588456
2531591560
2531592036
2531592037
2531592046
2531593872
2531594457
2531594475
2531594481
2531594503
2531594515
2531597664
2531597713
2531597717
2531597726
2531597795
2531597806
2531597809
2531597810
2531597820
2531599836
2531605356
2531605390
UDI:
05415334026810
Product: NexxisOR MNA-620 DEC -H
Model / REF:
K9306210
Serial Numbers:
2531542260
2531542263
2531542270
2531542292
2531543553
2531543568
2531543588
2531582676
2531582691
2531588558
2531588562
2531593741
2531593749
2531593752
2531593763
2531593764
2531593768
2531593777
2531593784
2531595829
2531595831
2531601786
Product: NexxisOR MNA-620 ENC -H
Model / REF:
K9306220
Serial Numbers:
2531540107
2531542441
2531542470
2531543538
2531543549
2531543611
2531543613
2531543640
2531563132
2531572740
2531572759
2531572770
2531572814
2531572827
2531575652
2531594331
2531594332
2531594336
2531594348
2531594350
Product: NexxisOR MNA-640 DEC -H
Model / REF:
K9306410
Serial Numbers:
2531572228
2531582713
2531582724
2531582725
2531584168
2531584176
2531584191
2531588591
2531588593
2531588598
2531588616
2531588626
2531604519
2531604535
2531604544
2531604545
2531604549
2531604550
2531604551
2531604593
2531604637
2531604649
2531604658
Product: NexxisOR MNA-640 ENC -H
Model / REF:
K9306420
Serial Numbers:
2531537844
2531537870
2531537889
2531537901
2531537902
2531556037
2531556043
2531572419
2531572433
2531572440
2531595759

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 96885
Status: Active
Manufacturer: Barco N.V.
Sold By: Authorized Medical Device Distributors
Manufactured In: Belgium
Units Affected: 221
Distributed To: Texas, Ohio
Agency Last Updated: October 30, 2025

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

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This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.