Class II — Potential Health Hazard

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

BASE Recalled by SpineFrontier, Inc. Due to The S-LIFT Instrument Case contained a bracket with...

Date: May 17, 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

BASE, S-LIFT Instrument Case Product Usage: System cases are designed to hold and secure all instrumentation to be used with a surgical system. Case and caddy components are used to contain implants intended for intervertebral body fusion and fixation of the spine.

Quantity: 12

Why Was This Recalled?

The S-LIFT Instrument Case contained a bracket with peeling nylon coating.

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