Device recall
Z-1245-2026: Vortex Surgical 1. 23GA Laser Probe Curved Cat No. VS0120.23 2. 25GA Laser Probe…
FDA device recall · Class II · Vortex Surgical Inc.
Key facts
| Recall number (Z-number) | Z-1245-2026 |
|---|---|
| Recall event | 98255 |
| Product | Vortex Surgical 1. 23GA Laser Probe Curved Cat No. VS0120.23 2. 25GA Laser Probe Curved Cat No. VS0120.25 3. 25GA Laser Probe Flex-Tip Cat No. VS0130.25 4. 25GA Laser Probe Illuminated Curved Cat No. VS0125.25B 5. 25GA Laser Probe MaxReach Cat No. VS0140.25 6. 25GA Laser Probe Straight Cat No… |
| 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