Class II — Potential Health Hazard

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

StaXx¿ IB Convex Expandable Implant (25 x 12 x 9 mm) Recalled by Spine Wave, Inc. Due to A component Superior endplate manufactured from a different...

Date: May 14, 2013
Company: Spine Wave, 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 Spine Wave, Inc. directly.

Affected Products

StaXx¿ IB Convex Expandable Implant (25 x 12 x 9 mm), Intervertebral Fusion Device, Lumbar; Catalog Number 11 -1902. Indicated for intervertebral body fusion procedures in skeletally mature patients.

Quantity: 17 units

Why Was This Recalled?

A component Superior endplate manufactured from a different polymer than specified

Where Was This Sold?

This product was distributed to 2 states: FL, OR

Affected (2 states)Not affected

About Spine Wave, Inc.

Spine Wave, Inc. has 2 total recalls tracked by RecallDetector.

Related Recalls

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