Class II — Potential Health Hazard

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

Indus Invue Screws: IM71013-XX: Indus Screw04.0mm SelfDrilling. Used to secure Recalled by SpineFrontier, Inc. Due to Mismarked and unmarked screws

Date: November 20, 2013
Company: SpineFrontier, 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 SpineFrontier, Inc. directly.

Affected Products

Indus Invue Screws: IM71013-XX: Indus Screw04.0mm SelfDrilling. Used to secure the Invue Anterior Cervical Plate in position.

Quantity: N/A

Why Was This Recalled?

Mismarked and unmarked screws

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About SpineFrontier, Inc.

SpineFrontier, Inc. has 33 total recalls tracked by RecallDetector.

Related Recalls

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