Device recall
Z-1107-2023: TrackX Insight Base Modular Instrument Tracker, 5L, REF #604-3TX, Sterile; and…
FDA device recall · Class II · Trackx Technology Inc
Key facts
| Recall number (Z-number) | Z-1107-2023 |
|---|---|
| Recall event | 91338 |
| Product | TrackX Insight Base Modular Instrument Tracker, 5L, REF #604-3TX, Sterile; and TrackX Insight Base Modular Instrument Tracker, 6.5L, Model #605-3TX, Sterile. |
| Product code | OWB |
| Recalling firm | Trackx Technology Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 10, 2026 |
| 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