Device recall
Z-2261-2024: This product is a single use sterile device that is used to direct the lesion to…
FDA device recall · Class II · Stryker Corporation
Key facts
| Recall number (Z-number) | Z-2261-2024 |
|---|---|
| Recall event | 94755 |
| Product | This product is a single use sterile device that is used to direct the lesion to the targeted site. Each cannula contains a stylet that is removed once the cannula is placed. The electrode is then inserted into the cannula. Catalog Number: 0406-630-225 |
| Product code | GXI |
| Recalling firm | Stryker Corporation |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K032406 |
| FEI number | 3015967359 |
At a glance
- 1–9 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