# FDA recall Z-1994-2025

> **Barco N.V.** · Class II · device recall initiated 2025-05-09.

## Product

Model: Description/REF: MNA-420: MNA-420 ENC -H/K9303320, MNA-420 DEC -H V2/K9303331;   MNA-440: MNA-440 ENC -H/K9303300, MNA-440 DEC -H V2/K9303311;   MNA-620: MNA-620 DEC -H/K9306210, MNA-620 ENC -H/K9306220;   and MNA-640: MNA-640 DEC -H/K9306410, MNA-640 ENC -H/K9306420; components of the NexxisOR system

## Reason for recall

Cathode ray tube display system encoders and decoders have same MAC address; new system setup with two or more affected units can lead to systems not functioning reliably:audio, video and/or control signals might be interrupted or fall away, displays might switch to failover and back multiple times, devices/sources/sinks might not be discovered/available, might lead to delayed/prolonged procedures

## Distribution

US Nationwide distribution in the states of TX, OH.

## Key facts

- **Recall number:** Z-1994-2025
- **Recalling firm:** Barco N.V.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-05-09
- **Report date:** 2025-07-02

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Kortrijk, Belgium

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1994-2025

## Citation

> AI Analytics. FDA recall Z-1994-2025. Retrieved 2026-07-16 from https://api.ai-analytics.org/recall/Z-1994-2025. Source: US FDA. Licensed CC0.

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