Class II — Potential Health Hazard

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

Sterile Low Profile Screw Recalled by Arthrex, Inc. Due to Screws provided in packaging are 5mm shorter than...

Date: June 24, 2020
Company: Arthrex, 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 Arthrex, Inc. directly.

Affected Products

Sterile Low Profile Screw, Titanium, 6.7 x 65mm Part Number: AR-8967-2865S - Product Usage: is intended to be used as a stand-alone bone screw, or in a plate-screw system for internal bone fixation for bone fractures, fusions, osteotomies and non-unions.

Quantity: 28 units

Why Was This Recalled?

Screws provided in packaging are 5mm shorter than intended

Where Was This Sold?

International distribution in the countries of Denmark, United Kingdom, Sweden, Japan, Netherlands

About Arthrex, Inc.

Arthrex, Inc. has 28 total recalls tracked by RecallDetector.

Related Recalls

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