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Biomet Microfixation, LLC recalls Total Temporomandibular Joint Replacement System- 50mm Lft Standard Ti Mandi Reconstruction of the temporomandibular jo
Recalled December 17, 2014 · FDA recall Z-0518-2015 · Biomet Microfixation
Hazard
Laser etching on the parts is wider and deeper than the conditions previously validated. · FDA Class II
Units
42
Sold at
Worldwide Distribution - USA including PA, MN, CA and Internationally to Australia, Netherlands, France, and United Kingdom.
Description
Laser etching on the parts is wider and deeper than the conditions previously validated.
Product
Total Temporomandibular Joint Replacement System- 50mm Lft Standard Ti Mandi Reconstruction of the temporomandibular joint
Manufacturer(s)
Biomet Microfixation, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →