Device recall
Z-0260-2025: Product Name: Insight Base Flex - 8, Ref 608-3TX; The device consists of a…
FDA device recall · Class III · Trackx Technology Inc
Key facts
| Recall number (Z-number) | Z-0260-2025 |
|---|---|
| Recall event | 95424 |
| Product | Product Name: Insight Base Flex - 8, Ref 608-3TX; The device consists of a sterile Snap that includes reflective features that facilitate imaging of the (attached) instrument using instrument tracking technology when used with a compatible tracking system. Each TrackX Snap has a unique set of 2 or… |
| Product code | OWB |
| Recalling firm | Trackx Technology Inc |
| Recall class | Class III |
| Status | Open, Classified |
| 510(k) numbers | K173736, K200360 |
| FEI number | 3014391847 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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