Class II — Potential Health Hazard

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

APTUS 2.8 TriLock Screw 22mm Recalled by Medartis Inc. Due to Screw is 16mm long instead of 22mm long.

Date: April 12, 2024
Company: Medartis Inc.
Status: Ongoing
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 Medartis Inc. directly.

Affected Products

APTUS 2.8 TriLock Screw 22mm, HD7, 1/Pkg. Metal bone fixation fastener used with the APTUS fixation system.

Quantity: 110 units

Why Was This Recalled?

Screw is 16mm long instead of 22mm long.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Medartis Inc.

Medartis Inc. has 1 total recall tracked by RecallDetector.

Related Recalls

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