Exactech, Inc.: Medical Device Recall in 2017 - (Recall #: Z-3018-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: June 23, 2017

Date Posted: August 23, 2017

Recall Number: Z-3018-2017

Event ID: 77592

Reason for Recall:

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

Status: Terminated

Product Quantity: 68 devices

Code Information:

Catalog Number 02-029-29-1000, Lot Number 83843-001.

Distribution Pattern:

US Distribution to the states of : AZ, CA, CO, FL, IL, OH, OK, NV, NY, SC and TN.

Voluntary or Mandated:

Voluntary: Firm initiated