Device recall
Z-2486-2025: RefleXion X1 Model RXM1000 UDI Codes: (01)00860003983812(11)230504(21)X11001…
FDA device recall · Class II · Reflexion Medical, Inc.
Key facts
| Recall number (Z-number) | Z-2486-2025 |
|---|---|
| Recall event | 97311 |
| Product | RefleXion X1 Model RXM1000 UDI Codes: (01)00860003983812(11)230504(21)X11001 (01)00860003983812(11)230518(21)X11002 (01)00860003983812(11)230505(21)X11003 (01)00860003983812(11)230530(21)X11004 (01)00860003983812(11)230811(21)X11006 (01)00860003983812(11)230410(21)X11007… |
| Product code | QVA |
| Recalling firm | Reflexion Medical, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3011716550 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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