Lower risk Medical device recall · FDA · Published April 24, 2024

Barco MNA-420 HDMI Display Recall: HDMI Channel Inaccessible Due to SFP+ Module Issue

Barco recalls specific MNA-420 ENC HDMI units with material number K9303311 due to potential HDMI channel inaccessibility when connected to certain SFP+ modules. Affected units may not function properly.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-2332-2024Medical device Barco ›

Lower-risk recall

We have identified a potential issue with the SFP+ module supplied by Molex (Part Number: B620050) when connected to the ETH0 slot of either the MNA-6x0 ENC HDMI or MNA-4x0 ENC HDMI. In some instances, this connection may render the first HDMI channel inaccessible, making both the channel and the respective MNA ENC unit unusable. Additionally, readings from the module become unavailable when this issue arises. Similarly, when this Molex module is connected to the ETH0 slot of an MNA-620 ENC ANA, readings may also become inaccessible.

Take action

Contact the company

Recalling firmBarco N.V.President Kennedypark 35 · Kortrijk, Belgium

✎ GovInfoNow plain-language explainer

Barco is recalling specific MNA-420 ENC HDMI units with material number K9303311 because a faulty SFP+ module from Molex can cause the first HDMI channel to become inaccessible, making the unit unusable. This issue affects only certain serial numbers and does not pose a risk of injury. Read more at govinfonow.com/recall/55306-barco-mna-420-hdmi-display-recall-hdmi-channel-inaccessible-due.

Source Summary by GovInfoNow · govinfonow.com/recall/55306-barco-mna-420-hdmi-display-recall-hdmi-channel-inaccessible-due · Updated August 19, 2026 · FDA enforcement record: FDA #Z-2332-2024

Cite this page

“Barco MNA-420 HDMI Display Recall: HDMI Channel Inaccessible Due to SFP+ Module Issue.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/55306-barco-mna-420-hdmi-display-recall-hdmi-channel-inaccessible-due. Based on FDA recall #Z-2332-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2332-2024%22&limit=1).

The FDA announced on April 24, 2024, that Barco N.V. is recalling MNA-420 ENC HDMI cathode ray tube displays due to a potential issue with an SFP+ module that may render the unit unusable. The recall affects 88 units distributed in Florida.

How to tell if you have it

Brand: Barco
Product: MNA-420 ENC HDMI, Material Number K9303311; cathode ray tube display
Serial numbers: 2530986299 through 2530986327, 2531041594, 2531041591, 2531041578, 2531041585, 2531041595 through 2531041616, 2531041579, 2531041615, 2531041603, 2531041597, 2531041592, 2530985205, 2530986280 through 2530986298
Units affected: 88
Distribution: US: FL

The hazard

According to the FDA, a potential issue with the SFP+ module supplied by Molex (Part Number: B620050) may render the first HDMI channel inaccessible when connected to the ETH0 slot of specific MNA ENC units. This connection can make both the channel and the respective MNA ENC unit unusable, and readings from the module become unavailable. Similarly, when this Molex module is connected to the ETH0 slot of an MNA-620 ENC ANA, readings may also become inaccessible.

Context

GovInfoNow's records show Barco N.V. has had 3 other recalls on record since 2021-01-22. Other recent recalls of similar products include Barco MNA-420/440/620/640 Encoders/Decoders: Systems May Disconnect (2025-05-09) and Barco MDSC-8527 NXF Recall: I2C Cable Issue Blocks Decoder Function (2023-12-20).

How to tell if you have this one

Check if your MNA-420 ENC HDMI unit has material number K9303311 and one of the listed serial numbers. The recall covers specific units with these identifiers.

Brand
Barco
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Unit Details
Verify your unit's material number and serial number against the list provided in the recall notice.

Where it went and when

Where it was distributed

Distributed in Florida.

FDA distribution: “US: FL” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Florida.

Recall timeline

FDA published this recall 3 months after the firm started it.

Apr 24, 2024Firm started the recall
Jul 11, 2024FDA classified it Class II
Jul 17, 2024Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Link to this recall

<a href="https://govinfonow.com/recall/55306-barco-mna-420-hdmi-display-recall-hdmi-channel-inaccessible-due">Barco MNA-420 HDMI Display Recall: HDMI Channel Inaccessible Due to SFP+ Module Issue (GovInfoNow)</a>

Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #Z-2332-2024 (April 24, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2332-2024 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.