Class II — Potential Health Hazard

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

V. Mueller Neuro/Spine Recalled by Cardinal Health 200, LLC Due to Potential risk associated with corrosion demonstrated on the...

Date: September 23, 2016
Company: Cardinal Health 200, 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 Cardinal Health 200, LLC directly.

Affected Products

V. Mueller Neuro/Spine, SHADOW-LINE, SPINAL DISTRACTION SCREW, STERILE, various sizes (12mm, 14mm, 16mm and 18mm) 5 PER BOX.

Quantity: 72,076 units

Why Was This Recalled?

Potential risk associated with corrosion demonstrated on the distraction screw surface.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Cardinal Health 200, LLC

Cardinal Health 200, LLC has 275 total recalls tracked by RecallDetector.

Related Recalls

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