Class II — Potential Health Hazard

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

MaxAn 4.0mm and 4.5mm fixed screws Recalled by Biomet Spine, LLC Due to The packaging of 4.5 mm diameter MaxAn screws...

Date: September 29, 2015
Company: Biomet Spine, LLC
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 Biomet Spine, LLC directly.

Affected Products

MaxAn 4.0mm and 4.5mm fixed screws, used in the MaxAn Anterior Cervical Plate System. The MaxAn Anterior Cervical Plate System is a decompression-based technique for cervical spine stabilization.

Quantity: 17 units

Why Was This Recalled?

The packaging of 4.5 mm diameter MaxAn screws identifies/labels the screws as 4.0 mm diameter screws.

Where Was This Sold?

This product was distributed to 3 states: FL, MO, NY

Affected (3 states)Not affected

About Biomet Spine, LLC

Biomet Spine, LLC has 13 total recalls tracked by RecallDetector.

Related Recalls

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