Class II — Potential Health Hazard

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

Microline Renew Fenestrated Control Tip Grasper Recalled by Microline Surgical Due to Grasper jaw may break when force is applied...

Date: April 14, 2014
Company: Microline Surgical
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 Microline Surgical directly.

Affected Products

Microline Renew Fenestrated Control Tip Grasper, Single Patient Use, Product Number: 3222 The ReNew Fenestrated Grasper Forceps Tips are intended to cut, grasp, and dissect various abdominal tissue for use in endoscopic, including laproscopic surgical procedures where instruments are introduced onto the body through a cannula.

Quantity: 540 units

Why Was This Recalled?

Grasper jaw may break when force is applied to the jaw

Where Was This Sold?

This product was distributed to 4 states: IL, NY, TN, TX

Affected (4 states)Not affected

About Microline Surgical

Microline Surgical has 1 total recall tracked by RecallDetector.

Related Recalls

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