Device recall
Z-2237-2019: VAMPIRO V5001-minimally invasive poole suction sleeve that is an accessory…
FDA device recall · Class II · Santanello Surgical LLC
Key facts
| Recall number (Z-number) | Z-2237-2019 |
|---|---|
| Recall event | 83051 |
| Product | VAMPIRO V5001-minimally invasive poole suction sleeve that is an accessory instrument to ANY 5mm spot suction/irrigation catheter |
| Product code | JOL |
| Recalling firm | Santanello Surgical LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 13, 2021 |
| FEI number | 3013555389 |
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