Device recall
Z-1994-2025: Model: Description/REF: MNA-420: MNA-420 ENC -H/K9303320, MNA-420 DEC -H…
FDA device recall · Class II · Barco N.V.
Key facts
| Recall number (Z-number) | Z-1994-2025 |
|---|---|
| Recall event | 96885 |
| 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… |
| Product code | DXJ |
| Recalling firm | Barco N.V. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K173381 |
| FEI number | 3004455125 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database