Device recall
Z-0146-2014: da Vinci Vision System Cart, a component of the da Vinci Si Surgical System…
FDA device recall · Class III · Intuitive Surgical, Inc.
Key facts
| Recall number (Z-number) | Z-0146-2014 |
|---|---|
| Recall event | 66570 |
| Product | da Vinci Vision System Cart, a component of the da Vinci Si Surgical System IS3000; Y1903 Illuminator (Illuminator + Lamp Module); Y1902 Replacement Lamp Modules. Intuitive Surgical, Sunnyvale, CA. As a component of the IS3000 da Vinci Si Surgical System, the 3DHD Vision System provides a high… |
| Product code | NAY |
| Recalling firm | Intuitive Surgical, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Sep 4, 2014 |
| 510(k) numbers | K081137 |
| 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