Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Biomet Microfixation Temporomandibular Joint (TMJ) Patient Matched Left Fossa Part# Recalled by Biomet Microfixation, LLC Due to Product mix occurred prior to final package and...
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 Biomet Microfixation, LLC directly.
Affected Products
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.
Quantity: 1
Why Was This Recalled?
Product mix occurred prior to final package and labeling process.
Where Was This Sold?
Worldwide Distribution to Denmark only.
About Biomet Microfixation, LLC
Biomet Microfixation, LLC has 19 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report