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Biomet 3i, LLC recalls BIOMET 3i Endosseous Dental Implant.
Recalled April 23, 2014 · FDA recall Z-1458-2014 · Biomet 3i
Hazard
Due to residual machining fluid identified by discoloration (darker in appearance) on the external dental implant surface. · FDA Class II
Units
34,744
Sold at
Worldwide Distribution - USA and countries of United Arab Emirates, Argentina, Austria, Australia, Belgium, Brazil, Canada, Switzerland, Chile, Colombia, Costa Rica, Germany, Dominican Republic, Spain, France, Great Britain (UK), Greece, Hong Kong, Ireland, Israel, India, Italy, Japan, Korea (South), Lebanon, Liechtenstein, Lithuania, Mexico, Netherlands, Poland, Portugal, Paraguay, Saudi Arabia, Sweden, Singapore, Turkey, Taiwan, Uruguay, Vietnam and South Africa.
Description
Due to residual machining fluid identified by discoloration (darker in appearance) on the external dental implant surface.
Product
BIOMET 3i Endosseous Dental Implant.
Manufacturer(s)
Biomet 3i, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →