Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Da Vinci 5 ASSY Recalled by Intuitive Surgical, Inc. Due to An error event following the release of a...

Date: November 17, 2025
Company: Intuitive Surgical, Inc.
Status: Ongoing
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Intuitive Surgical, Inc. directly.

Affected Products

Da Vinci 5 ASSY, DV5 CONSOLE, IS5000 Model/Catalog Number: 380730 Used for minimally invasive surgery.

Quantity: 12

Why Was This Recalled?

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.

Where Was This Sold?

This product was distributed to 6 states: LA, MA, NY, PA, TX, VA

Affected (6 states)Not affected

About Intuitive Surgical, Inc.

Intuitive Surgical, Inc. has 244 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report