Class II — Potential Health Hazard

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

Truliant Tibial Trial Handle. To assist the surgeon in the Recalled by Exactech, Inc. Due to The Truliant Tibial Trial Handle's pin may disassociate...

Date: June 23, 2017
Company: Exactech, 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 Exactech, Inc. directly.

Affected Products

Truliant Tibial Trial Handle. To assist the surgeon in the implantation of Truliant Knee system components according to a conventional technique for total knee replacement. Specifically, these instruments are reusable, surgically invasive, and intended for transient use.t Tibial Trial Handle

Quantity: 68 devices

Why Was This Recalled?

The Truliant Tibial Trial Handle's pin may disassociate from the main body.

Where Was This Sold?

This product was distributed to 11 states: AZ, CA, CO, FL, IL, NV, NY, OH, OK, SC, TN

Affected (11 states)Not affected

About Exactech, Inc.

Exactech, Inc. has 211 total recalls tracked by RecallDetector.

Related Recalls

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