Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
BIOMET 3i Endosseous Dental Implant. Recalled by Biomet 3i, LLC Due to Due to residual machining fluid identified by discoloration...
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 3i, LLC directly.
Affected Products
BIOMET 3i Endosseous Dental Implant.
Quantity: 34,744
Why Was This Recalled?
Due to residual machining fluid identified by discoloration (darker in appearance) on the external dental implant surface.
Where Was This Sold?
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.
About Biomet 3i, LLC
Biomet 3i, LLC has 222 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report