Class II — Potential Health Hazard

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

Brand Name: N/A Product Name: Repeater Bone Tamp Model/Catalog Number: Recalled by Integrity Implants Inc. Due to Due to incompatibility of bone tamp (Rev A)...

Date: December 20, 2024
Company: Integrity Implants Inc.
Status: Ongoing
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 Integrity Implants Inc. directly.

Affected Products

Brand Name: N/A Product Name: Repeater Bone Tamp Model/Catalog Number: ASY-00132 Software Version: N/A Product Description: The Repeater Bone Tamp is a cylindrical shaft used to push bone graft material through a corresponding bone funnel into the FlareHawk interbody fusion device in spinal fusion procedures. Component: No

Quantity: 9

Why Was This Recalled?

Due to incompatibility of bone tamp (Rev A) and bone funnels (Rev C).

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Integrity Implants Inc.

Integrity Implants Inc. has 6 total recalls tracked by RecallDetector.

Related Recalls

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