Device recall
Z-2342-2018: Safety Sideport Knife 1.0mm 45, REF 378210 Product Usage: Indicated to make stab…
FDA device recall · Class II · Beaver Visitec
Key facts
| Recall number (Z-number) | Z-2342-2018 |
|---|---|
| Recall event | 80311 |
| Product | Safety Sideport Knife 1.0mm 45, REF 378210 Product Usage: Indicated to make stab incisions during ophthalmic surgery |
| Product code | EMF |
| Recalling firm | Beaver Visitec |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 8, 2021 |
| FEI number | 1211998 |
At a glance
- None 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