Device recall
Z-1210-2022: DAVINCI | Energy SynchroSeal da Vinci X' da Vinci Xi', Single Use Instrument…
FDA device recall · Class II · Intuitive Surgical, Inc.
Key facts
| Recall number (Z-number) | Z-1210-2022 |
|---|---|
| Recall event | 89641 |
| Product | DAVINCI | Energy SynchroSeal da Vinci X' da Vinci Xi', Single Use Instrument 8mm, REF 480440 |
| Product code | GEI |
| Recalling firm | Intuitive Surgical, Inc. |
| Recall class | Class II |
| Status | Completed |
| 510(k) numbers | K191280 |
| FEI number | 3001675293 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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