MNA-420 ENC HDMI, Material Number K9303311 recallZ-2332-2024 · Barco N.V. · initiated Apr 24, 2024
Class II Completed All recalls posted in July 2024
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from Barco N.V. or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
Why it was recalled
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.
FDA root cause category: Other
What the company is doing
Barco NV notified its sole consignee on 04/29/2024 via email. The notice explained the issue, potential risk, and requested the following: "Actions to be taken by the customer: 1. Identify the location and amount of all Molex modules that are listed in pdf document Molex_SN_Partner . 2. Fill out and send back Response Form 1 to your Barco Key Account Manager, including the number of distributed units per country. 3. Disable or discard all used Molex modules. 4. Fill out and send back Response Form 2 to your Barco Key Account Manager after completion of the actions. For question, contact your Barco Key Account Manager.
Recall details
- Recall number
- Z-2332-2024
- Recall class
- Class II
- Status
- Completed
- Initiated by the company
- Apr 24, 2024
- Posted by the FDA
- Jul 11, 2024
- Recalling firm
- Barco N.V.
- Quantity
- 88 units
- Product code
- DXJ
- FDA submissions
- K173381
- Distribution
- US: FL
Product description
MNA-420 ENC HDMI, Material Number K9303311; cathode ray tube display
Code information (models, lots, serial numbers)
Show the full code information (1k characters)
serial numbers: 2530986299, 2530986300, 2530986301, 2530986302, 2530986303, 2530986304, 2530986305, 2530986306, 2530986307, 2530986308, 2530986309, 2530986310, 2530986311, 2530986312, 2530986313, 2530986314, 2530986315, 2530986316, 2530986317, 2530986318, 2530986319, 2530986320, 2530986321, 2530986322, 2530986323, 2530986324, 2530986325, 2530986326, 2530986327, 2531041594, 2531041591, 2531041578, 2531041585, 2531041595, 2531041596, 2531041586, 2531041588, 2531041587, 2531041577, 2531041584, 2531041581, 2531041612, 2531041608, 2531041600, 2531041601, 2531041604, 2531041599, 2531041602, 2531041605, 2531041606, 2531041607, 2531041609, 2531041610, 2531041580, 2531041583, 2531041598, 2531041593, 2531041590, 2531041614, 2531041582, 2531041613, 2531041589, 2531041616, 2531041579, 2531041615, 2531041603, 2531041597, 2531041592, 2530985205, 2530986280, 2530986281, 2530986282, 2530986283, 2530986284, 2530986285, 2530986286, 2530986287, 2530986288, 2530986289, 2530986290, 2530986291, 2530986292, 2530986293, 2530986294, 2530986295, 2530986296, 2530986297, 2530986298
Other devices under the same FDA submission
4 devices cleared under K173381 — the recall does not name any of them by identifier. One submission often covers many models, so they may or may not be affected.
- Nexxis MNA-440Barco NV · DISPLAY, CATHODE-RAY TUBE, MEDICAL1 recall0 reports
- Nexxis MNA-420Barco NV · DISPLAY, CATHODE-RAY TUBE, MEDICAL1 recall0 reports
- Nexxis OR MNA-440 DECBarco NV · DISPLAY, CATHODE-RAY TUBE, MEDICAL1 recall0 reports
- Nexxis OR MNA-420 DECBarco NV · DISPLAY, CATHODE-RAY TUBE, MEDICAL1 recall0 reports
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 18, 2026. Text above is shown as published by the FDA.
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