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Biomet Microfixation, LLC recalls Biomet Microfixation Temporomandibular Joint (TMJ) Patient Matched Left Fossa Part# CP751506 The Total Temporomandib
Recalled September 10, 2014 · FDA recall Z-2566-2014 · Biomet Microfixation
Hazard
Product mix occurred prior to final package and labeling process. · FDA Class II
Units
1
Sold at
Worldwide Distribution to Denmark only.
Description
Product mix occurred prior to final package and labeling process.
Product
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.
Manufacturer(s)
Biomet Microfixation, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →