Device recall
Z-2278-2020: Genicon GENILook Model 200-105-252, 5mm diameter, 150mm length (2 cannula)…
FDA device recall · Class II · Genicon, Inc.
Key facts
| Recall number (Z-number) | Z-2278-2020 |
|---|---|
| Recall event | 85407 |
| Product | Genicon GENILook Model 200-105-252, 5mm diameter, 150mm length (2 cannula) - Product Usage: The universal handle can be used as a pistol grip or like a traditional Trocar handle when using a scope. |
| Product code | GEA |
| Recalling firm | Genicon, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K982472 |
| FEI number | 3002590791 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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