CLASS II ONGOING Device recall · Reported 5 Oct 2022 · FDA Enforcement Report
Medical Network Adapter, MNA-240, part of the NexxisOR system recalled
Barco Nv is recalling Barco Medical Network Adapter, MNA-240, part of the NexxisOR system, distributed nationwide in the US. The recall was initiated on 27 Jul 2022 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-1854-2022
- FDA event ID
- 90807
- Recalling firm
- Barco Nv, Kortrijk, N/A
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 27 Jul 2022
- FDA classified
- 29 Sep 2022
- Reported
- 5 Oct 2022
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Other Reasons
- Device type
- Other Medical Devices
Timeline
| 27 Jul 2022 | Recall initiated by company | |
| 29 Sep 2022 | Classified by FDA | +64 days |
| 5 Oct 2022 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
installation issues
Product as listed by the FDA
Barco Medical Network Adapter, MNA-240, part of the NexxisOR system, Model Numbers: a) K9303078A, b) K9303097A
Where it was distributed
US Nationwide distribution in the states of FL, IL, NJ.
Questions about this recall
Is Medical Network Adapter, MNA-240, part of the NexxisOR system recalled?
Yes. Barco Nv recalled Medical Network Adapter, MNA-240, part of the NexxisOR system on 27 Jul 2022. The recall is Class II and its status is Ongoing. Recall number Z-1854-2022.
Why was it recalled?
installation issues
Which lots are affected?
a) K9303078A, UDI 05415334000056, all serial numbers; b) K9303097A, UDI 05415334001657, all serial numbers
Where was it sold?
US Nationwide distribution in the states of FL, IL, NJ.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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