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MNA-420 ENC HDMI, Material Number K9303311; cathode ray tube display

FDA Device Recall #Z-2332-2024 — Class II — April 24, 2024

Recall Summary

Recall Number Z-2332-2024
Classification Class II — Moderate risk
Date Initiated April 24, 2024
Status Completed
Voluntary Voluntary: Firm initiated

Recalling Firm

Firm Barco N.V.
Location Kortrijk, N/A
Product Type Devices
Quantity 88 units

Product Description

MNA-420 ENC HDMI, Material Number K9303311; cathode ray tube display

Reason for 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.

Distribution Pattern

US: FL

Lot / Code Information

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 Recalls from Barco N.V.

Recall # Classification Product Date
Z-1994-2025 Class II Model: Description/REF: MNA-420: MNA-420 ENC -H... May 9, 2025
Z-0979-2024 Class II Barco MDSC-8527 NXF, Part Number K9352421 Dec 20, 2023
Z-1172-2021 Class II Barco MDNC-3421 DISPLAY, DIAGNOSTIC RADIOLOGY Jan 22, 2021
Z-0527-2019 Class II Optional MDRC-1119 Front Cover Attachment Kit ... Mar 30, 2017

Frequently Asked Questions

Contact your healthcare provider and the device manufacturer immediately. Check whether your specific model number and lot number are included in the recall scope. For external devices, stop using the affected product and arrange a replacement. For implanted devices, do not panic — removal is typically not required unless the risk assessment clearly indicates it. Your physician will guide you based on your individual clinical situation and the FDA's recommended actions. Report any adverse effects you may have experienced to FDA MedWatch at 1-800-FDA-1088.

Class I recalls indicate a reasonable probability of serious adverse health consequences or death from the defect. Class II recalls involve products that may cause temporary or medically reversible adverse health consequences, or where serious consequences are remote. Class III recalls cover products not likely to cause any adverse health consequences, typically involving technical regulatory violations. The classification guides urgency — Class I recalls require immediate action, while Class III may simply involve returning a product or acknowledging a labeling change. Always read the specific recall notice for recommended patient actions.

Report problems with medical devices to the FDA through MedWatch at 1-800-FDA-1088 or online at FDA.gov/safety/medwatch. Healthcare facilities are required by law to report device-related serious injuries and deaths. Patients and consumers can also report voluntarily. Include the device name, manufacturer, model number, and a description of the problem and any patient outcome. Reports from patients and clinicians help the FDA identify emerging safety signals and may trigger investigations that lead to recalls of dangerous devices.

What Should You Do?

Stop using this device if you are affected by this recall. Contact your healthcare provider and the manufacturer immediately for guidance. Report adverse events to FDA MedWatch.

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