FDA Medical Device Recalls (openFDA)
Barco N.V.: MNA-420 ENC HDMI, Material Number K9303311; cathode ray tube display
- Recall number
- Z-2332-2024
- Recalling firm
- Barco N.V.
- Product
- MNA-420 ENC HDMI, Material Number K9303311; cathode ray tube display
- Status
- Completed
- Initiated
- 2024-04-24
- Posted
- 2024-07-11
- Terminated
- not on file
- Reason
- 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.
- Root cause
- Other
- Action
- 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.
- Quantity
- 88 units
- Distribution
- US: FL
- Lot, serial or model codes
- 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
- 510(k) numbers
- K173381
- PMA numbers
- not on file
- Product code
- DXJ
- Firm FEI
- 3004455125
- Firm city
- Kortrijk
- Firm state
- not on file
- Firm country
- Belgium
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28