Device recall
Z-1769-2025: KliniTray Platte Faxitron,groB "R" sterile. Tissue resection margin examination…
FDA device recall · Class II · Klinika Mdical Gmb
Key facts
| Recall number (Z-number) | Z-1769-2025 |
|---|---|
| Recall event | 96656 |
| Product | KliniTray Platte Faxitron ,groB "R" sterile. Tissue resection margin examination board/large Model Number: 2001155-F The medical device KliniTrayTM is a system for the precise monitoring, recording and visualization of alignment during surgical procedures. It ensures the exact orientation and… |
| Product code | FMH |
| Recalling firm | Klinika Mdical Gmb |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3008352701 |
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