Class II — Potential Health Hazard

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

GMK Intramedullary Extension Rod 100 mm is a rod to Recalled by Medacta Usa Due to Medacta has registered in its database 3 cases...

Date: September 22, 2014
Company: Medacta Usa
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 Medacta Usa directly.

Affected Products

GMK Intramedullary Extension Rod 100 mm is a rod to obtain correct leg alignment during total knee replacement. Rod to obtain correct leg alignment during total knee replacement.

Quantity: 1 rod (US); 145 rods (global)

Why Was This Recalled?

Medacta has registered in its database 3 cases of breakage of the GMK Intramedullary Extension Rod 100 mm, code 02.07.10.0162.

Where Was This Sold?

This product was distributed to 1 state: OH

Affected (1 state)Not affected

About Medacta Usa

Medacta Usa has 3 total recalls tracked by RecallDetector.

Related Recalls

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