Device recall
Z-0500-2018: bvi Beaver EdgeAhead Safety Knife, (a) Sideport MVR.90mm 20G, REF 370531 (b)…
FDA device recall · Class II · Beaver-Visitec International Inc.
Key facts
| Recall number (Z-number) | Z-0500-2018 |
|---|---|
| Recall event | 78789 |
| Product | bvi Beaver EdgeAhead Safety Knife, (a) Sideport MVR .90mm 20G, REF 370531 (b) Sideport Angled, .60mm (23G), REF 378233 Product Usage: Specialty blades and knives are used for stab and cut incisions in ophthalmic, ENT and other surgical applications. |
| Product code | EMF |
| Recalling firm | Beaver-Visitec International Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 31, 2023 |
| 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