Device recall
Z-0040-2026: EverPatch+, REF: 1044002, Permanent Scleral Reinforcement Matrix 1x5.0mm x 8.5…
FDA device recall · Class II · CORNEAT VISION, LTD.
Key facts
| Recall number (Z-number) | Z-0040-2026 |
|---|---|
| Recall event | 97463 |
| Product | EverPatch+, REF: 1044002, Permanent Scleral Reinforcement Matrix 1x5.0mm x 8.5 mm Shield/1 x 5.0mm x 6.5 mm Rectangle, STERILE VH202 |
| Product code | QWU |
| Recalling firm | CORNEAT VISION, LTD. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K223074 |
| FEI number | 3029772936 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 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