Class II — Potential Health Hazard

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

Insight Instruments MIS ( Multi-Port Illumination System) Illuminated pilot tubes Recalled by Insight Instruments, Inc. Due to Insight Instruments, Inc., Stuart, FL is recalling M.I.S....

Date: March 15, 2013
Company: Insight Instruments, 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 Insight Instruments, Inc. directly.

Affected Products

Insight Instruments MIS ( Multi-Port Illumination System) Illuminated pilot tubes work like a ceiling light while simultaneously protecting the entry sites. Illumination automatically follows the movement of the two surgical instruments inserted into the M.I.S. cannulas. The large distance of more than 16mm between cannula ends and posterior pole guarantees sufficient light in the working area and a large observation field especially when used in conjunction with modern wide field panoramic observation systems.

Quantity: 776

Why Was This Recalled?

Insight Instruments, Inc., Stuart, FL is recalling M.I.S. (Multi-Port Illumination System), Ophthalmic Cannula due to a misclassification of the medical device.

Where Was This Sold?

This product was distributed to 2 states: IL, IN

Affected (2 states)Not affected

About Insight Instruments, Inc.

Insight Instruments, Inc. has 3 total recalls tracked by RecallDetector.

Related Recalls

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