Device recall
Z-0798-2025: Ivalon Eye Wick 20cm- Intended to be used for the removal and collection of…
FDA device recall · Class II · Carwild Corporation
Key facts
| Recall number (Z-number) | Z-0798-2025 |
|---|---|
| Recall event | 95909 |
| Product | Ivalon Eye Wick 20cm- Intended to be used for the removal and collection of fluids from the Opthalmic surgical site. Model Number: Q604206 |
| Product code | HOZ |
| Recalling firm | Carwild Corporation |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K971832 |
| FEI number | 1219313 |
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