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 Xi Surgical System Recalled by Intuitive Surgical, Inc. Due to Due to a manufacturing variation in the arm...

Date: November 21, 2018
Company: Intuitive Surgical, Inc.
Status: Terminated
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 Xi Surgical System

Quantity: 74 USMs containing affected rotors.

Why Was This Recalled?

Due to a manufacturing variation in the arm that can result in a persistent recoverable fault error (error 23087) and loss of arm functionality prior or during surgery.

Where Was This Sold?

This product was distributed to 13 states: CA, DE, FL, IL, KY, MD, MA, MI, NJ, NY, OH, TX, VA

Affected (13 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