Device recall
Z-0799-2025: Ivalon CELLULOSE SURGICAL SPEAR- Intended To Be Used During Ophthalmic Surgical…
FDA device recall · Class II · Carwild Corporation
Key facts
| Recall number (Z-number) | Z-0799-2025 |
|---|---|
| Recall event | 95909 |
| Product | Ivalon CELLULOSE SURGICAL SPEAR- Intended To Be Used During Ophthalmic Surgical Procedures For Fluid Management Model Number: Q604237 |
| 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