Device recall
Z-1246-2026: Oertli 1. 23G Laser Probe OS4 Flex-Tip VK401113 2. 23G Laser Probe OS4…
FDA device recall · Class II · Vortex Surgical Inc.
Key facts
| Recall number (Z-number) | Z-1246-2026 |
|---|---|
| Recall event | 98255 |
| Product | Oertli 1. 23G Laser Probe OS4 Flex-Tip VK401113 2. 23G Laser Probe OS4 Illuminated Flex-Tip VK401213 3. 23G Laser Probe OS4 Intuitive Exendable VK401323 4. 25G Laser Probe OS4 Flex-Tip VK401115 5. 25G Laser Probe OS4 Illuminated Flex-Tip VK401215 6. 25G Laser Probe OS4 Intuitive Exendable VK401325… |
| Product code | HQB |
| Recalling firm | Vortex Surgical Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K220263 |
| FEI number | 3013002167 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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