Device recall
Z-1111-2019: Beaver Xstar Slit Knife 2.4 mm, 45degree Double Bevel, Ophthalmic-utilized in…
FDA device recall · Class II · Beaver Visitec
Key facts
| Recall number (Z-number) | Z-1111-2019 |
|---|---|
| Recall event | 82382 |
| Product | Beaver Xstar Slit Knife 2.4 mm, 45degree Double Bevel, Ophthalmic-utilized in Cataract and Glaucoma procedures REF # 370824 Product Usage: Ophthalmic techniques-utilized in Cataract and Glaucoma procedures |
| Product code | HNN |
| Recalling firm | Beaver Visitec |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 11, 2020 |
| 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