Device recall
Z-1803-2015: BVI Custom Eyes Ophthalmic Procedure Kits with the component -Devon Light Glove…
FDA device recall · Class II · Beaver-Visitec International Inc.
Key facts
| Recall number (Z-number) | Z-1803-2015 |
|---|---|
| Recall event | 71293 |
| Product | BVI Custom Eyes Ophthalmic Procedure Kits with the component -Devon Light Glove Part Number: 584648 Ophthalmic surgical kits |
| Product code | FSY |
| Recalling firm | Beaver-Visitec International Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 28, 2021 |
| FEI number | 1211998 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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