Class II — Potential Health Hazard

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

Straight Impactor - Dorado IBC Recalled by SpineFrontier, Inc. Due to During two separate occasions an impactor plate on...

Date: May 10, 2008
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

Straight Impactor - Dorado IBC, Part Number: SI02140. The device is used to position implants after they have been inserted into the disc space during implantation of intervertebral body fusion devices.

Quantity: 10

Why Was This Recalled?

During two separate occasions an impactor plate on the handle broke off while being struck by a mallet.

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