Device recall
Z-1244-2026: Volk Single Use Vitrectomy Lenses 1. Flat Vitrectomy Lens, Catalog VFD 2. Volk…
FDA device recall · Class II · Vortex Surgical Inc.
Key facts
| Recall number (Z-number) | Z-1244-2026 |
|---|---|
| Recall event | 98255 |
| Product | Volk Single Use Vitrectomy Lenses 1. Flat Vitrectomy Lens, Catalog VFD 2. Volk Magnifying Lens, Catalog VMD |
| Product code | HJK |
| Recalling firm | Vortex Surgical Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K050623 |
| FEI number | 3013002167 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 Products in the same recall event
- 1–9 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