Class II — Potential Health Hazard

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

Cannula 8MM Regular. Provides the means of introduction and placement Recalled by Intuitive Surgical, Inc. Due to Clarification of existing labeling information and operating procedures.

Date: September 19, 2011
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

Cannula 8MM Regular. Provides the means of introduction and placement of an instrument or accessory into the human body.

Quantity: NA

Why Was This Recalled?

Clarification of existing labeling information and operating procedures.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 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