Device recall
Z-3034-2026: ORT300, operating room table, ORT300 Modular Table Main Unit Assy Part Numbers…
FDA device recall · Class II · IMRIS Imaging Inc
Key facts
| Recall number (Z-number) | Z-3034-2026 |
|---|---|
| Recall event | 99596 |
| Product | ORT300, operating room table, ORT300 Modular Table Main Unit Assy Part Numbers 114093-000 and 114093-600 |
| Product code | KXJ |
| Recalling firm | IMRIS Imaging Inc |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3010326005 |
At a glance
- None 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