Biomet Microfixation, LLC: Medical Device Recall in 2014 - (Recall #: Z-0517-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

Total Temporomandibular Joint Replacement System- 50mm Rt Standard Ti Mand Reconstruction of the temporomandibular joint

Product Classification:

Class II

Date Initiated: October 17, 2014

Date Posted: December 17, 2014

Recall Number: Z-0517-2015

Event ID: 69644

Reason for Recall:

Laser etching on the parts is wider and deeper than the conditions previously validated.

Status: Terminated

Product Quantity: 42

Code Information:

Model 24-6650TI, Lot #s: 518480B, 518480A, 525970A, 525970B, 525980B, 518490A, 526070A, 525990A, 525990B, 526060A, 526060B, 526070B, 525980A, 550330A, 550330B, 550340A, 550340B, 550350A, 550360A, 550360B, 518490B, 525960A, 525960B,

Distribution Pattern:

Worldwide Distribution - USA including PA, MN, CA and Internationally to Australia, Netherlands, France, and United Kingdom.

Voluntary or Mandated:

Voluntary: Firm initiated