Device recall
Z-0229-2022: bvi CustomEyes Kit-Lafayette General Medical Center: CustomEyes Cataract…
FDA device recall · Class II · Beaver Visitec International, Inc.
Key facts
| Recall number (Z-number) | Z-0229-2022 |
|---|---|
| Recall event | 88826 |
| Product | bvi CustomEyes Kit-Lafayette General Medical Center: CustomEyes Cataract Surgical Kits that contain Beaver Xstar Crescent Knife (REF#373809) as a component REF# 58000572 REF#: 373809 |
| Product code | OJK |
| Recalling firm | Beaver Visitec International, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 1211998 |
At a glance
- None Linked 510(k)s
- 1–9 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