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Biomet 3i, LLC recalls CERTAIN BELLATEK TIN ABUTMENT 4.1MM Reference Number: IEDAN4
Recalled October 14, 2020 · FDA recall Z-0075-2021 · Biomet 3i
Hazard
Hex of the BellaTek Encode Definitive Abutments was misaligned by 30 degrees during manufacturing as compared with the provided patient scan data (Images may cause misalignment, the definitive abutment will not seat in the correct orientation upon attempted placement with the patient · FDA Class II
Units
9 units
Sold at
FL, GA, ID, IL, MI, NV, NY, OH, SC, TN, VA
Description
Hex of the BellaTek Encode Definitive Abutments was misaligned by 30 degrees during manufacturing as compared with the provided patient scan data (Images may cause misalignment, the definitive abutment will not seat in the correct orientation upon attempted placement with the patient
Product
CERTAIN BELLATEK TIN ABUTMENT 4.1MM Reference Number: IEDAN4
Manufacturer(s)
Biomet 3i, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →