Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
3i T3 Non-Platform Switched Tapered Implant Rx Only Recalled by Biomet 3i, LLC Due to Endosseous Dental Implants in contact with a residual...
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
3i T3 Non-Platform Switched Tapered Implant Rx Only; 3.25 x 8.5 - 15.0 mm Dental Implants.
Quantity: 620 implants in total
Why Was This Recalled?
Endosseous Dental Implants in contact with a residual machine fluid caused the implants to be discolored.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
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