Class II — BARCO NV
| Recalling firm | BARCO NV |
|---|---|
| Registered facility | View this company's 5 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | installation issues |
| Product | Barco Medical Network Adapter, MNA-240, part of the NexxisOR system, Model Numbers: a) K9303078A, b) K9303097A |
| Quantity | 169 devices |
| Distribution | US Nationwide distribution in the states of FL, IL, NJ. |
| Initiated | 2022-07-27 |
| Classified | 2022-09-29 |
| Recall number | Z-1854-2022 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — BARCO NV (Z-1854-2022).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/90807/
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