Barco cathode ray tube display may lose connectivity with Molex module installed
Barco display units may lose HDMI connectivity and become unusable when a specific Molex network module is installed in the ETH0 slot of affected models.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: FDA Class II medical device with a connectivity defect causing device non-functionality. No injuries, illnesses, or reported incidents documented in the source. The hazard is operational loss rather than direct patient safety risk.
Plain-English summary
Barco N.V. is recalling 88 MNA-420 ENC HDMI cathode ray tube display units due to a connectivity issue involving an SFP+ module supplied by Molex.
When the Molex module (Part Number B620050) is connected to the ETH0 slot of the affected display units, the connection may render the first HDMI channel inaccessible. This defect makes both the channel and the display unit unusable, and readings from the module become unavailable.
The affected units are identified by specific serial numbers and were distributed in Florida.
Customers who own affected units should verify their serial numbers against the provided recall list. If your unit is affected, discontinue use of the Molex module in the ETH0 slot or contact Barco N.V. for instructions on replacement or repair options.
The recalled product
- Product
- MNA-420 ENC HDMI, Material Number K9303311; cathode ray tube display
- Manufacturer
- Barco N.V.
- Hazard
- connectivity-issue
- device-malfunction
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (20)
- serial numbers: 2530986299
- 2530986300
- 2530986301
- 2530986302
- 2530986303
- 2530986304
- 2530986305
- 2530986306
- 2530986307
- 2530986308
- 2530986309
- 2530986310
- 2530986311
- 2530986312
- 2530986313
- 2530986314
- 2530986315
- 2530986316
- 2530986317
- 2530986318
Distribution
Distributed in 1 state:
- FL
Related recalls
Same category
- SevereMedtronic DLP Retrograde Cannula recalled for sterile barrier breach risk
FDA (Devices) · 2026-05-27
- HighSwan-Ganz Jr Catheter models recalled due to lumen hub leakage
FDA (Devices) · 2026-05-27
- HighAzurion X-ray System Deaeration Hose May Degrade and Cause Oil Leakage
FDA (Devices) · 2026-05-27
- HighMedtronic DLP Retrograde Cannula Cardiopulmonary Bypass Catheter Recall
FDA (Devices) · 2026-05-27
- HighMedtronic DLP Retrograde Cannula cardiopulmonary bypass catheter
FDA (Devices) · 2026-05-27