Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Osseotite 2 Certain Prevail 5mm(D)X 4.1mm (P) X X 11.5mm Recalled by Biomet 3i, LLC Due to One of the dental implants do not have...
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
Osseotite 2 Certain Prevail 5mm(D)X 4.1mm (P) X X 11.5mm (L) Dental Implant Product Usage: Surgical placement in the upper or lower jaw to provide a means for prosthetic attachment in single tooth restorations and in partially or fully edentulous spans with multiple single teeth utilizing delayed or immediate loading or with a terminal or intermediary abutment for fixed or removable bridgework and to retain over dentures.
Quantity: 215
Why Was This Recalled?
One of the dental implants do not have the internal hex feature. One of the dental implants do not have the internal thread feature.
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