Device recall
Z-2439-2020: Control Panel REF - 60-02-50: LivaNova SCP Pump Control Panel S5/C5. REF…
FDA device recall · Class II · LivaNova Deutschland GmbH
Key facts
| Recall number (Z-number) | Z-2439-2020 |
|---|---|
| Recall event | 85505 |
| Product | Control Panel REF - 60-02-50: LivaNova SCP Pump Control Panel S5/C5. REF 60-02-50, IPX2, RxOnly, UDI: 04033817900993 |
| Product code | DWA |
| Recalling firm | LivaNova Deutschland GmbH |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 22, 2021 |
| 510(k) numbers | K011838 |
| FEI number | 3002808267 |
At a glance
- 1–9 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