Device recall
Z-0182-04: Ronci Surgical Universal Imaging Extension used with the Ronci Pain Management…
FDA device recall · Class II · The OR Group
Key facts
| Recall number (Z-number) | Z-0182-04 |
|---|---|
| Recall event | 27655 |
| Product | Ronci Surgical Universal Imaging Extension used with the Ronci Pain Management Table System Catalog Number: R-934-25A |
| Product code | FPS |
| Recalling firm | The OR Group |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 25, 2005 |
| FEI number | 1221538 |
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