Biomet Microfixation, LLC: Medical Device Recall in 2014 - (Recall #: Z-2566-2014)

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:

Biomet Microfixation Temporomandibular Joint (TMJ) Patient Matched Left Fossa Part# CP751506 The Total Temporomandibular Joint (TMJ) replacement system is implanted in the jaw to functionally reconstruct a diseased and/or damaged temporomandibular joint. The Total TMJ replacement system is a two-component system comprised of mandibular condyle and a glenoid fossa components. Both components are available in multiple stock sizes as right and left specific designs and are attached to the bones by screws.

Product Classification:

Class II

Date Initiated: September 20, 2013

Date Posted: September 10, 2014

Recall Number: Z-2566-2014

Event ID: 67547

Reason for Recall:

Product mix occurred prior to final package and labeling process.

Status: Terminated

Product Quantity: 1

Code Information:

Part #CP751506 Lot #478490

Distribution Pattern:

Worldwide Distribution to Denmark only.

Voluntary or Mandated:

Voluntary: Firm initiated