Recall
Da Vinci 5 ASSY, DV5 CONSOLE, IS5000 Model/Catalog Number: 380730 Used for minimally invasive surgery.
Intuitive Surgical, Inc. · 17 Nov 2025
- Status
- Recall open, classified
- Why, in the FDA's words
- “An error event following the release of a software version for the surgical system that can result in loss of user interface content on an external monitor or tower monitor.”
- Recall began
- 17 Nov 2025
- Company
- Intuitive Surgical, Inc.
- Device type
- Robot-assisted surgical systems (computer-controlled instruments) (NAY)
- Concerns
- K232610
What it means
A recall is the FDA's record that a company is correcting or removing a device because of a problem. Many are fixed with a software update or new instructions; the record does not say whether anyone was hurt. See our plain guide to FDA terms.
The record
The FDA publishes this record in its public device database. The summary documents the company filed, when available, are linked from the FDA's page.