Skip to content

Nexxis MNA-240 (REF K9303097A)Recalls & reported problems

Barco NV · MNA-240 ENC DP MQ · Class 2

All models of Nexxis (4)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.

Adverse event reports
0
Deaths reported
0
Injuries reported
0
Recalls naming it
1

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

1 FDA recall record name this device's identifier, 1 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Recalls naming this device

  1. Jul 27, 2022Open, Classified

    installation issues

    Z-1854-2022 · Root cause: Labeling design · Recall details · FDA record ↗

Other DISPLAY, CATHODE-RAY TUBE, MEDICAL devices

All DISPLAY, CATHODE-RAY TUBE, MEDICAL devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page